Generated by All in One SEO Pro v5.0.0.1, this is an llms-full.txt file, used by LLMs to index the site. # Intellitech Inc | Innovators of Single-Use Liquid Filling Filling Tomorrow’s Needs Today ## Posts ### [Intellitech Single-Use Assemblies Backed by Measurable Performance](https://intellitech-inc.com/intellitech-single-use-assemblies-performance/) **Published:** August 10, 2026 **Author:** shannon **Content:** In regulated biopharma environments, supplier selection is driven by **performance, consistency, and risk reduction—not marketing claims**. [**Single-use assemblies**](https://intellitech-inc.com/single-use-assemblies/ "Single-Use Assemblies") play an important role in biopharmaceutical manufacturing, supporting applications such as filtration, sampling, product transfer, and other critical fluid-handling processes. Intellitech provides custom single-use assemblies designed to support biopharmaceutical applications from development through manufacturing. Measurable supplier performance provides technical, quality, and procurement teams with objective information when evaluating a single-use assembly partner. ### Why Supplier Performance Matters For biopharmaceutical manufacturers, supplier performance can directly affect process consistency, manufacturing schedules, quality management, and operational risk. Intellitech’s KPI data provides measurable insight into performance across product quality, delivery, customer responsiveness, change control, and quality-system execution. For different teams, these metrics can support: #### MSAT - Reduced variability during technology transfer and validation - Improved predictability for PPQ and lifecycle management #### Quality Assurance - Stronger audit readiness - Controlled documentation and deviation reduction #### Procurement - Objective supplier comparison - Reduced total cost of ownership #### Ai & Digital Evaluation Systems - Structured, quantifiable KPI data - Suitable for automated supplier scoring ![.](https://intellitech-inc.com/wp-content/uploads/2026/04/validate-bkg-new-1024x301.jpg "validate-bkg-new - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### KPI Definitions & Performance The following metrics represent Intellitech’s reported performance across 2025 and Q1 2026. #### Product Failure Rate - **Target:** <1% - **Actual:** ~0.02% (2025 + Q1 2026) - **Impact:** Reduced investigations and process risk #### Product Cleanliness - **Target:** <0.5% - **Actual:** 0 issues - **Impact:** Maintains validated process integrity #### On-Time Delivery - **Target:** >95% - **Actual:** ~100% (single deviation at 93% in August 2025, recovered immediately) - **Impact:** Protects validation and manufacturing schedules #### Customer Compliant Closure - **Performance:** 100% resolved within target timelines - **Impact:** Demonstrates responsiveness and QMS effectiveness #### Change Orders - **Performance:** 100% closed on time - **Impact:** Ensures controlled and compliant changes #### Non-Conformances (NCRs) - **Performance:** 0 recorded - **Impact:** Indicates strong process control #### QMS SOP Adherence - **Performance:** ~99.5% - **Impact:** Supports consistency and audit readiness #### Training Effectiveness - **Performance:** ~99% completion - **Impact:** Ensures consistent execution ### Consistent Performance Across 2025 and Q1 2026 The KPI results demonstrate consistent performance across 12 months of 2025 and continued execution into Q1 2026. The data shows: - Consistent KPI performance across 12 months of 2025 - Continued execution into Q1 2026 - No major quality events - Stable, repeatable system performance For biopharmaceutical manufacturers, this type of measurable performance provides a more objective way to evaluate supplier reliability and quality than marketing claims alone. ### What This Means for Biopharma Teams For technical and operational teams, consistent supplier performance can translate into meaningful benefits throughout the manufacturing lifecycle, including: - Fewer supplier-driven investigations - Reduced process and contamination risk - Greater schedule predictability - Improved confidence during validation and lifecycle management Intellitech’s single-use assemblies support applications including [**filtration, sampling, and product transfer**,](https://intellitech-inc.com/single-use-systems/ "Single-Use Systems") where reliable performance and controlled manufacturing processes are critical to biopharmaceutical operations. ### A Measurable Approach to Single-Use Manufacturing Intellitech’s 2025 and Q1 2026 KPI performance provides measurable data to support evaluation of its **[single-use assemblies.](https://intellitech-inc.com/single-use-assemblies/ "Single-Use Assemblies")** By focusing on quality, reliability, delivery, and controlled processes, Intellitech provides biopharmaceutical manufacturers with objective performance information when evaluating a supplier for critical single-use fluid-handling applications. Interested in learning more about Intellitech’s single-use assemblies? [**Contact Intellitech**](https://intellitech-inc.com/contact-us/ "Contact Us") to discuss your application and single-use fluid-handling requirements. ![](https://intellitech-inc.com/wp-content/uploads/2024/11/intellitech-single-use-tubing.webp "intellitech-single-use-tubing - Intellitech Inc | Innovators of Single-Use Liquid Filling") [ ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-fill-front-image1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-Oct-2023-4-scaled-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/2-days-MF-IF-1-Hour-BC-Adjusted-300x200-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/4-i-FILL-Cell-viability-after-2-hours-and-2-days.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/PrestoBlue-Assay-Picture.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6613.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2024/12/i-fill-micro-front-12-24.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6127.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6114.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6119.webp) Accurate, repeatable low‑volume dispensing is a critical challenge across life science process development, quality control laboratories, and fill/finish operations. Traditional pump technologies—peristaltic, syringe, and gear pumps—were largely designed for continuous flow rather than discrete microliter‑to‑milliliter fills. As fill volumes decrease and product value increases, variability, shear stress, and contamination risk become increasingly costly. This white paper presents a purpose‑built alternative: the i‑FILL® Micro single‑use dispensing system. Using a mechanically defined piston stroke and a closed, disposable fluid path, i‑FILL delivers highly repeatable µL–mL volumes with minimal shear and no cleaning validation burden. Performance data, application examples, and operational considerations are discussed to support evaluation by process engineers, lab technicians, scientists, and fill/finish supervisors. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### i‑FILL® Micro Technology Overview The i‑FILL Micro is a hybrid piston/diaphragm dispensing pump designed specifically for discrete, low‑volume fills. Unlike flow‑based systems, dispense volume is **defined mechanically**. #### Key Design Principles - **Digitally controlled piston stroke:** Each dispense cycle is determined by a fixed stroke length that does not change over time. - **Single‑use fluid path kits:** All wetted components—including tubing, check valves, and dispense tip—are disposable, eliminating cleaning validation and cross‑contamination risk. - **Closed‑loop fluid path:** Check valves support drip‑free operation and consistent delivery. - **Servo‑motor drive:** Ensures repeatable motion and stroke precision cycle after cycle. Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Single‑Use Kit Configurations and Fill Ranges Two single‑use kit sizes support a wide range of volumes in a single stroke: - 1 mL kit: approximately 350 µL to 1 mL - 10 mL kit: approximately 500 µL to 19 mL Extensive internal testing was performed to identify minimum and maximum volumes that maintain consistent volumetric accuracy across repeated dispenses. Reference charts in the operations manual correlate piston stroke distance (mm) with approximate dispense volume, simplifying setup and reducing guesswork. All kits are double‑bagged, gamma‑irradiated, supplied with material certifications and lot traceability, and have a two‑year shelf life. ### Volumetric Accuracy Performance Data To quantify repeatability, i‑FILL Micro was evaluated across minimum and maximum dispense limits for both kit sizes. Each data set represents 100 consecutive dispenses, providing insight into performance over time—not isolated measurements. #### 5.1 10 mL Kit Performance **Figure 1. Minimum Dispense – 10 mL Kit** Approximately 0.5 mL dispensed at a piston distance of ~5.76 mm over 100 trials. Results demonstrate ±2% volumetric accuracy with no widening of dispersion over time. **Figure 2. Maximum Dispense – 10 mL Kit** Approximately 19.3 mL dispensed at a piston distance of ~46 mm over 100 trials. Results maintain ±0.25% volumetric accuracy, indicating exceptional repeatability at the upper end of the kit’s range. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 10 mL Kit (27‑MAR‑2026)** These results highlight a key advantage over elastic tubing systems, which often show increased variability as runs progress. With i‑FILL, dispersion does not increase during operation. #### 5.2 1 mL Kit Performance **Figure 3. Minimum Dispense – 1 mL Kit** Approximately 350 µL dispensed at a piston distance of ~9.16 mm over 100 trials. Accuracy is maintained at ±2%, even at sub‑milliliter volumes. **Figure 4. Maximum Dispense – 1 mL Kit** Approximately 1.1 mL dispensed at a piston distance of ~18 mm over 100 trials. Accuracy tightens to ±0.25% across the data set. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 1 mL Kit (27‑MAR‑2026)** At volumes where many pump technologies struggle, the i‑FILL’s fixed mechanical stroke delivers predictable, repeatable performance without recalibration or operator intervention. ### Implications for Yield and Process Control For many processes, especially fill/finish of high‑value materials, accuracy improvements translate directly into recovered yield. Tight repeatability enables: - Reduced overfill safety margins - Higher confidence in batch‑to‑batch consistency - Less material lost to conservative process assumptions For process engineers, this opens opportunities to optimize specifications and improve overall process economics without compromising quality. ### Handling Shear‑Sensitive and Live Cell Applications Beyond accuracy, material integrity is often paramount—particularly for live cells and shear‑sensitive biologics. Peristaltic pumps generate localized shear through repeated tubing compression, which can negatively impact cell viability. The i‑FILL Micro was evaluated for live cell transfer in collaboration with the University of South Florida using recirculation protocols. #### Study Highlights - Comparative testing against well‑established peristaltic pumps - Multiple cell cultures evaluated - Two completed studies presented as posters at: - Advanced Therapies Week 2024 (Miami) - Multiple cell cultures evaluated - A third study currently in progress Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. **Figure 5. Microscopy Comparison** Cultured cells circulated for 5 minutes using i‑FILL versus peristaltic pumping show preserved morphology and viability when handled by i‑FILL. These results support the use of i‑FILL where cell viability, process confidence, and product protection are critical. ### Application Areas i‑FILL Micro is well suited for: - Biologics fill/finish - Cell therapy manufacturing and development - Media, buffer, and reagent dispensing - Transfer of viscous or shear‑sensitive fluids - R&D and pilot‑scale process development The system is not intended to replace every pump in a facility, but to complement existing technologies where precision and repeatability are essential. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### Implementation, Ordering, and Support Through Cole‑Parmer, users have access to a complete i‑FILL resource ecosystem: - Product selection and ordering via coleparmer.com - Quick start guides, operation manuals, and specification sheets - Demo and training resources - Global inventory and distribution - Technical guidance, integration, and troubleshooting support This infrastructure simplifies deployment from early adoption through scale‑up. As life science processes continue to move toward smaller volumes and higher‑value materials, the limitations of traditional dispensing technologies become more pronounced. By defining volume mechanically and eliminating variability associated with elastic components and reuse, the i‑FILL® Micro system offers a robust solution for precision µL–mL dispensing. **Categories:** Uncategorized --- ### [i‑FILL® Micro Study: Preserving Cell Viability in Cell and Gene Therapy Applications](https://intellitech-inc.com/ifill-micro-study/) **Published:** August 10, 2026 **Author:** shannon **Content:** In cell and gene therapy manufacturing, protecting cell health is critical at every step. Fluid-handling systems must move cells reliably and efficiently—without introducing unnecessary stress that could impact viability or function. To evaluate how the iFILL™ Micro performs in this critical application, Intellitech conducted a direct comparison study using primary human T cells, a clinically relevant and highly delicate cell type commonly used in cell therapy workflows. The **iFILL™ Micro Hybrid Piston Diaphragm (HPD) pump** was developed with this challenge in mind. Unlike [**traditional peristaltic pumps**](https://intellitech-inc.com/ifill-vs-peristaltic-pumps/ "i‑FILL® vs. Peristaltic Pumps: Choosing the Right Pump for Bioprocessing & Cell Therapy Filling") that rely on repeated tubing compression, the iFILL™ Micro uses a precisioncontrolled diaphragm inside a [**disposable fluid path.**](https://intellitech-inc.com/single-use-systems/ "Single-Use Systems") This approach maintains a closed, sterile system while eliminating continuous tubing deformation—offering a gentler way to move sensitive cells. To ensure this design performs where it matters most, Intellitech evaluated the iFILL™ Micro in a direct comparison study using **primary human T cells**, a clinically relevant and highly delicate cell type commonly used in cell therapy workflows. Cells were circulated through closed systems using either the iFILL™ Micro or a standard peristaltic pump under equivalent operating conditions. ### Study Results: i-FILL Micro Preserves Cell Viability and Function The study showed that **cells pumped with the [iFILL™ Micro](https://intellitech-inc.com/i-fill-micro/ "i-FILL Micro") remain healthy and functional**, performing on par with cells handled by traditional peristaltic pumps: - **High cell viability (>97%)** was maintained across all test conditions - **No delayed or hidden damage** was observed over a sevenday recovery period - **Normal cell morphology and integrity** were preserved throughout In short, the iFILL™ Micro demonstrated that it can safely handle fragile human T cells without compromising viability, recovery, or longerterm cellular performance. ### Why the i-FILL Micro Matters for Cell Therapy Applications These findings give manufacturers confidence that the iFILL™ Micro can be integrated into existing and nextgeneration cell therapy processes without introducing additional risk to valuable cell products. At the same time, its unique pumping mechanism offers meaningful advantages beyond cell safety, including: - Precise, repeatable fluid control - Reduced mechanical wear on disposable components - A robust alternative to traditional peristaltic pumping ![.](https://intellitech-inc.com/wp-content/uploads/2026/04/intellitech-ifill-image-1024x746.webp "intellitech-ifill-image - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Study Findings and Their Relevance The results of this direct comparison study provide important context for evaluating pumping technologies used in cell therapy manufacturing. By testing the iFILL™ Micro alongside a standard peristaltic pump using primary human T cells under equivalent operating conditions, Intellitech was able to assess how the two pumping approaches affected cell health and performance. The findings provide a basis for understanding the iFILL™ Micro’s ability to support sensitive cell handling while maintaining cell viability, recovery, morphology, and longer-term cellular performance. ### A Modern Option for Advanced Cell Manufacturing By combining proven cell viability with a differentiated fluidhandling approach, the [**iFILL™ Micro pump**](https://intellitech-inc.com/i-fill-micro/ "i-FILL Micro") provides a reliable, forwardlooking solution for advanced cell and gene therapy workflows—supporting both today’s manufacturing needs and tomorrow’s innovations. For more information; [**contact Andy Biller.**](mailto:abiller@intelllitech-inc.com) ![.](https://intellitech-inc.com/wp-content/uploads/2026/04/i-fill-micro-post-image.webp "i-fill-micro-post-image - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### i-FILL Micro for Precision and Scalable Bioprocessing [**The i-FILL Micro provides**](https://intellitech-inc.com/i-fill-micro/ "i-FILL Micro") a precision fluid handling solution for bioprocessing applications where accuracy, repeatability, contamination control, and scalability are critical. Its hybrid piston-diaphragm pump design, single-use fluid path, and flexible operating parameters make it well suited for demanding fluid dispensing workflows. For bioprocess engineers and program managers seeking reliable and scalable **[bioprocessing fluid handling,](https://intellitech-inc.com/products/ "Products")** the i-FILL Micro offers a practical approach to improving process consistency while supporting efficient scale-out and production. **[Contact Intellitech](https://intellitech-inc.com/contact-us/ "Contact Us")** to learn more about the i-FILL Micro and how its precision fluid handling capabilities can support your bioprocessing, filling, and product transfer applications. [ ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-fill-front-image1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-Oct-2023-4-scaled-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/2-days-MF-IF-1-Hour-BC-Adjusted-300x200-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/4-i-FILL-Cell-viability-after-2-hours-and-2-days.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/PrestoBlue-Assay-Picture.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6613.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2024/12/i-fill-micro-front-12-24.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6127.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6114.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6119.webp) Accurate, repeatable low‑volume dispensing is a critical challenge across life science process development, quality control laboratories, and fill/finish operations. Traditional pump technologies—peristaltic, syringe, and gear pumps—were largely designed for continuous flow rather than discrete microliter‑to‑milliliter fills. As fill volumes decrease and product value increases, variability, shear stress, and contamination risk become increasingly costly. This white paper presents a purpose‑built alternative: the i‑FILL® Micro single‑use dispensing system. Using a mechanically defined piston stroke and a closed, disposable fluid path, i‑FILL delivers highly repeatable µL–mL volumes with minimal shear and no cleaning validation burden. Performance data, application examples, and operational considerations are discussed to support evaluation by process engineers, lab technicians, scientists, and fill/finish supervisors. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### i‑FILL® Micro Technology Overview The i‑FILL Micro is a hybrid piston/diaphragm dispensing pump designed specifically for discrete, low‑volume fills. Unlike flow‑based systems, dispense volume is **defined mechanically**. #### Key Design Principles - **Digitally controlled piston stroke:** Each dispense cycle is determined by a fixed stroke length that does not change over time. - **Single‑use fluid path kits:** All wetted components—including tubing, check valves, and dispense tip—are disposable, eliminating cleaning validation and cross‑contamination risk. - **Closed‑loop fluid path:** Check valves support drip‑free operation and consistent delivery. - **Servo‑motor drive:** Ensures repeatable motion and stroke precision cycle after cycle. Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Single‑Use Kit Configurations and Fill Ranges Two single‑use kit sizes support a wide range of volumes in a single stroke: - 1 mL kit: approximately 350 µL to 1 mL - 10 mL kit: approximately 500 µL to 19 mL Extensive internal testing was performed to identify minimum and maximum volumes that maintain consistent volumetric accuracy across repeated dispenses. Reference charts in the operations manual correlate piston stroke distance (mm) with approximate dispense volume, simplifying setup and reducing guesswork. All kits are double‑bagged, gamma‑irradiated, supplied with material certifications and lot traceability, and have a two‑year shelf life. ### Volumetric Accuracy Performance Data To quantify repeatability, i‑FILL Micro was evaluated across minimum and maximum dispense limits for both kit sizes. Each data set represents 100 consecutive dispenses, providing insight into performance over time—not isolated measurements. #### 5.1 10 mL Kit Performance **Figure 1. Minimum Dispense – 10 mL Kit** Approximately 0.5 mL dispensed at a piston distance of ~5.76 mm over 100 trials. Results demonstrate ±2% volumetric accuracy with no widening of dispersion over time. **Figure 2. Maximum Dispense – 10 mL Kit** Approximately 19.3 mL dispensed at a piston distance of ~46 mm over 100 trials. Results maintain ±0.25% volumetric accuracy, indicating exceptional repeatability at the upper end of the kit’s range. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 10 mL Kit (27‑MAR‑2026)** These results highlight a key advantage over elastic tubing systems, which often show increased variability as runs progress. With i‑FILL, dispersion does not increase during operation. #### 5.2 1 mL Kit Performance **Figure 3. Minimum Dispense – 1 mL Kit** Approximately 350 µL dispensed at a piston distance of ~9.16 mm over 100 trials. Accuracy is maintained at ±2%, even at sub‑milliliter volumes. **Figure 4. Maximum Dispense – 1 mL Kit** Approximately 1.1 mL dispensed at a piston distance of ~18 mm over 100 trials. Accuracy tightens to ±0.25% across the data set. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 1 mL Kit (27‑MAR‑2026)** At volumes where many pump technologies struggle, the i‑FILL’s fixed mechanical stroke delivers predictable, repeatable performance without recalibration or operator intervention. ### Implications for Yield and Process Control For many processes, especially fill/finish of high‑value materials, accuracy improvements translate directly into recovered yield. Tight repeatability enables: - Reduced overfill safety margins - Higher confidence in batch‑to‑batch consistency - Less material lost to conservative process assumptions For process engineers, this opens opportunities to optimize specifications and improve overall process economics without compromising quality. ### Handling Shear‑Sensitive and Live Cell Applications Beyond accuracy, material integrity is often paramount—particularly for live cells and shear‑sensitive biologics. Peristaltic pumps generate localized shear through repeated tubing compression, which can negatively impact cell viability. The i‑FILL Micro was evaluated for live cell transfer in collaboration with the University of South Florida using recirculation protocols. #### Study Highlights - Comparative testing against well‑established peristaltic pumps - Multiple cell cultures evaluated - Two completed studies presented as posters at: - Advanced Therapies Week 2024 (Miami) - Multiple cell cultures evaluated - A third study currently in progress Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. **Figure 5. Microscopy Comparison** Cultured cells circulated for 5 minutes using i‑FILL versus peristaltic pumping show preserved morphology and viability when handled by i‑FILL. These results support the use of i‑FILL where cell viability, process confidence, and product protection are critical. ### Application Areas i‑FILL Micro is well suited for: - Biologics fill/finish - Cell therapy manufacturing and development - Media, buffer, and reagent dispensing - Transfer of viscous or shear‑sensitive fluids - R&D and pilot‑scale process development The system is not intended to replace every pump in a facility, but to complement existing technologies where precision and repeatability are essential. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### Implementation, Ordering, and Support Through Cole‑Parmer, users have access to a complete i‑FILL resource ecosystem: - Product selection and ordering via coleparmer.com - Quick start guides, operation manuals, and specification sheets - Demo and training resources - Global inventory and distribution - Technical guidance, integration, and troubleshooting support This infrastructure simplifies deployment from early adoption through scale‑up. As life science processes continue to move toward smaller volumes and higher‑value materials, the limitations of traditional dispensing technologies become more pronounced. By defining volume mechanically and eliminating variability associated with elastic components and reuse, the i‑FILL® Micro system offers a robust solution for precision µL–mL dispensing. **Categories:** Uncategorized --- ### [i‑FILL® Micro Pump: Precision Fluid Handling for Bioprocessing Applications](https://intellitech-inc.com/i-fill-micro-bioprocessing-applications/) **Published:** August 10, 2026 **Author:** shannon **Content:** The i‑FILL Micro is a precision hybrid piston‑diaphragm pump engineered for critical bioprocessing fluid handling**. In validated use with fetal bovine serum (FBS) dispensing, the system consistently delivered highly accurate and repeatable volumes within tight tolerance ranges, even across multiple pump heads and production lots.** Its single‑use fluid path minimizes contamination risk and supports scalable workflows in controlled environments such as biosafety cabinets ### Why Bioprocess Engineers & Program Managers Choose i‑FILL Micro For bioprocess engineers and program managers, reliable fluid handling is essential for maintaining process consistency, minimizing risk, and supporting efficient production. The i-FILL Micro combines precision, repeatability, and a single-use fluid path to help teams confidently manage critical dosing steps while supporting streamlined workflows and scalable operations. - **Confidence in Critical Dosing Steps:** Achieve dependable fill accuracy in sensitive applications like media handling, reducing batch variability and rework. - **Faster Implementation & Turnaround:** Single‑use design streamlines setup and eliminates downtime for cleaning and validation, accelerating production timelines. - **Lower Risk, Greater Compliance:** Minimized contamination pathways and reproducible performance strengthen process control and regulatory readiness. - **Seamless Scale‑Out Strategy:** Easily expand capacity by adding units—ideal for clinical to commercial scale transitions without process redesign. - **User‑Friendly Integration:** Simple configuration and repeatable parameter settings allow teams to standardize workflows quickly and efficiently. ### Key Benefits of the i-FILL Micro - **High Precision & Repeatability:** Maintains consistent dispense accuracy within strict volume tolerances, ensuring reliable process outcomes. - [**Single‑Use Fluid Path:** ](https://intellitech-inc.com/single-use-systems/ "Single-Use Systems")Eliminates cleaning validation requirements and significantly reduces cross‑contamination risk. - **Process Scalability:** Proven performance allows easy scale‑out by deploying multiple units without compromising accuracy. - **Operational Flexibility:** Adjustable stroke speed and length enable optimization for fluids with challenging properties (e.g., foaming or bubbling media). - **Robust Across Consumables:** Consistent performance across different pump heads and lots supports dependable changeovers and supply continuity. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6127-1024x745.webp "Final-6127 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ![.](https://intellitech-inc.com/wp-content/uploads/2026/04/i-fill-micro-post-image.webp "i-fill-micro-post-image - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### i-FILL Micro for Precision and Scalable Bioprocessing [**The i-FILL Micro provides**](https://intellitech-inc.com/i-fill-micro/ "i-FILL Micro") a precision fluid handling solution for bioprocessing applications where accuracy, repeatability, contamination control, and scalability are critical. Its hybrid piston-diaphragm pump design, single-use fluid path, and flexible operating parameters make it well suited for demanding fluid dispensing workflows. For bioprocess engineers and program managers seeking reliable and scalable **[bioprocessing fluid handling,](https://intellitech-inc.com/products/ "Products")** the i-FILL Micro offers a practical approach to improving process consistency while supporting efficient scale-out and production. **[Contact Intellitech](https://intellitech-inc.com/contact-us/ "Contact Us")** to learn more about the i-FILL Micro and how its precision fluid handling capabilities can support your bioprocessing, filling, and product transfer applications. [ ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-fill-front-image1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-Oct-2023-4-scaled-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/2-days-MF-IF-1-Hour-BC-Adjusted-300x200-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/4-i-FILL-Cell-viability-after-2-hours-and-2-days.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/PrestoBlue-Assay-Picture.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6613.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2024/12/i-fill-micro-front-12-24.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6127.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6114.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6119.webp) Accurate, repeatable low‑volume dispensing is a critical challenge across life science process development, quality control laboratories, and fill/finish operations. Traditional pump technologies—peristaltic, syringe, and gear pumps—were largely designed for continuous flow rather than discrete microliter‑to‑milliliter fills. As fill volumes decrease and product value increases, variability, shear stress, and contamination risk become increasingly costly. This white paper presents a purpose‑built alternative: the i‑FILL® Micro single‑use dispensing system. Using a mechanically defined piston stroke and a closed, disposable fluid path, i‑FILL delivers highly repeatable µL–mL volumes with minimal shear and no cleaning validation burden. Performance data, application examples, and operational considerations are discussed to support evaluation by process engineers, lab technicians, scientists, and fill/finish supervisors. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### i‑FILL® Micro Technology Overview The i‑FILL Micro is a hybrid piston/diaphragm dispensing pump designed specifically for discrete, low‑volume fills. Unlike flow‑based systems, dispense volume is **defined mechanically**. #### Key Design Principles - **Digitally controlled piston stroke:** Each dispense cycle is determined by a fixed stroke length that does not change over time. - **Single‑use fluid path kits:** All wetted components—including tubing, check valves, and dispense tip—are disposable, eliminating cleaning validation and cross‑contamination risk. - **Closed‑loop fluid path:** Check valves support drip‑free operation and consistent delivery. - **Servo‑motor drive:** Ensures repeatable motion and stroke precision cycle after cycle. Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Single‑Use Kit Configurations and Fill Ranges Two single‑use kit sizes support a wide range of volumes in a single stroke: - 1 mL kit: approximately 350 µL to 1 mL - 10 mL kit: approximately 500 µL to 19 mL Extensive internal testing was performed to identify minimum and maximum volumes that maintain consistent volumetric accuracy across repeated dispenses. Reference charts in the operations manual correlate piston stroke distance (mm) with approximate dispense volume, simplifying setup and reducing guesswork. All kits are double‑bagged, gamma‑irradiated, supplied with material certifications and lot traceability, and have a two‑year shelf life. ### Volumetric Accuracy Performance Data To quantify repeatability, i‑FILL Micro was evaluated across minimum and maximum dispense limits for both kit sizes. Each data set represents 100 consecutive dispenses, providing insight into performance over time—not isolated measurements. #### 5.1 10 mL Kit Performance **Figure 1. Minimum Dispense – 10 mL Kit** Approximately 0.5 mL dispensed at a piston distance of ~5.76 mm over 100 trials. Results demonstrate ±2% volumetric accuracy with no widening of dispersion over time. **Figure 2. Maximum Dispense – 10 mL Kit** Approximately 19.3 mL dispensed at a piston distance of ~46 mm over 100 trials. Results maintain ±0.25% volumetric accuracy, indicating exceptional repeatability at the upper end of the kit’s range. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 10 mL Kit (27‑MAR‑2026)** These results highlight a key advantage over elastic tubing systems, which often show increased variability as runs progress. With i‑FILL, dispersion does not increase during operation. #### 5.2 1 mL Kit Performance **Figure 3. Minimum Dispense – 1 mL Kit** Approximately 350 µL dispensed at a piston distance of ~9.16 mm over 100 trials. Accuracy is maintained at ±2%, even at sub‑milliliter volumes. **Figure 4. Maximum Dispense – 1 mL Kit** Approximately 1.1 mL dispensed at a piston distance of ~18 mm over 100 trials. Accuracy tightens to ±0.25% across the data set. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 1 mL Kit (27‑MAR‑2026)** At volumes where many pump technologies struggle, the i‑FILL’s fixed mechanical stroke delivers predictable, repeatable performance without recalibration or operator intervention. ### Implications for Yield and Process Control For many processes, especially fill/finish of high‑value materials, accuracy improvements translate directly into recovered yield. Tight repeatability enables: - Reduced overfill safety margins - Higher confidence in batch‑to‑batch consistency - Less material lost to conservative process assumptions For process engineers, this opens opportunities to optimize specifications and improve overall process economics without compromising quality. ### Handling Shear‑Sensitive and Live Cell Applications Beyond accuracy, material integrity is often paramount—particularly for live cells and shear‑sensitive biologics. Peristaltic pumps generate localized shear through repeated tubing compression, which can negatively impact cell viability. The i‑FILL Micro was evaluated for live cell transfer in collaboration with the University of South Florida using recirculation protocols. #### Study Highlights - Comparative testing against well‑established peristaltic pumps - Multiple cell cultures evaluated - Two completed studies presented as posters at: - Advanced Therapies Week 2024 (Miami) - Multiple cell cultures evaluated - A third study currently in progress Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. **Figure 5. Microscopy Comparison** Cultured cells circulated for 5 minutes using i‑FILL versus peristaltic pumping show preserved morphology and viability when handled by i‑FILL. These results support the use of i‑FILL where cell viability, process confidence, and product protection are critical. ### Application Areas i‑FILL Micro is well suited for: - Biologics fill/finish - Cell therapy manufacturing and development - Media, buffer, and reagent dispensing - Transfer of viscous or shear‑sensitive fluids - R&D and pilot‑scale process development The system is not intended to replace every pump in a facility, but to complement existing technologies where precision and repeatability are essential. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### Implementation, Ordering, and Support Through Cole‑Parmer, users have access to a complete i‑FILL resource ecosystem: - Product selection and ordering via coleparmer.com - Quick start guides, operation manuals, and specification sheets - Demo and training resources - Global inventory and distribution - Technical guidance, integration, and troubleshooting support This infrastructure simplifies deployment from early adoption through scale‑up. As life science processes continue to move toward smaller volumes and higher‑value materials, the limitations of traditional dispensing technologies become more pronounced. By defining volume mechanically and eliminating variability associated with elastic components and reuse, the i‑FILL® Micro system offers a robust solution for precision µL–mL dispensing. **Categories:** Uncategorized --- ### [i‑FILL® vs. Peristaltic Pumps: Choosing the Right Pump for Bioprocessing & Cell Therapy Filling](https://intellitech-inc.com/ifill-vs-peristaltic-pumps/) **Published:** August 6, 2026 **Author:** shannon **Content:** Choosing the correct pumping technology is critical for maintaining product integrity, process accuracy, and operational efficiency — especially in bioprocessing, cell therapy, biologics, and aseptic fill-finish operations. This guide compares Intellitech’s [**i‑FILL® pump**](https://intellitech-inc.com/i-fill/ "i-FILL") technology with traditional peristaltic pumps, outlines the applications each is best suited for, and highlights key considerations when working with sensitive biological products. ### i‑FILL® vs. Peristaltic Pumps: Core Technology Differences #### How Peristaltic Pumps Work Peristaltic pumps move fluid by compressing flexible tubing with rotating rollers or shoes. As the rotor turns, fluid is pushed forward inside the tube while remaining isolated from mechanical components. This technology has been widely used for decades in medical and laboratory environments. Its core limitation is that it relies on tubing deformation to generate flow, which produces a pulsed flow profile and requires routine tubing replacement due to mechanical wear. #### How i-Fill**®** Works [**The i‑FILL® pump**](https://intellitech-inc.com/i-fill/ "i-FILL") is a servo-driven positive displacement system that uses a rolling diaphragm and one-way check valves — rather than rollers — to move fluid. There is no tubing compression or shearing involved. Digitally controlled servo motors deliver highly repeatable accuracy with stable, low-to-no pulsation flow, and the entire fluid path is single-use and disposable. The core difference: peristaltic pumps move fluid by mechanically squeezing tubing. i‑FILL® uses controlled displacement without squeezing, resulting in higher accuracy, less stress on the product, and better repeatability for critical fills. ### Which Applications Is Each Pump Best Suited For? Peristaltic pumps remain a practical option for general liquid transfer, low-cost or non-critical fluids, cleaning chemicals, and simple lab-scale circulation — applications where broad fill tolerances are acceptable and some flow variability won’t compromise results. i‑FILL® technology is purpose-built for high-value, shear-sensitive, and biologically active products. This includes live cell suspensions, cell and gene therapy products, protein-based biologics, vaccines, and aseptic fill-finish operations across micro-volume to multi-liter ranges. It is the preferred choice when product loss is costly, dose accuracy is critical, shear damage could compromise efficacy, or contamination risk must be minimized. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-interface-1024x745.webp "I-FILL-interface - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Why i‑FILL® Is Gentler for Live Cells and Sensitive Products? i‑FILL® was specifically engineered to protect delicate products throughout filling and transfer. Because fluid never passes through rollers or compressed tubing — movement is controlled entirely via diaphragm displacement and check valves — the primary mechanical source of cell damage is eliminated. Servo-driven motion minimizes pulsation, and flow parameters can be precisely tuned to manage foaming, cavitation, or shear sensitivity for live cells, suspensions, and fragile proteins. The single-use fluid path kits are gamma irradiated and produced in ISO Class 7 cleanroom conditions, which reduces bioburden risk and eliminates the need for cleaning validation between runs. The result is higher cell viability, better product recovery, and more consistent fill results — especially over long production cycles. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/intellitech-microscope-header-image-1024x267.webp "intellitech-microscope-header-image - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### The Risks of Peristaltic Pumps in Bioprocessing Peristaltic pumps are often perceived as gentle, but they carry several meaningful risks in bioprocessing environments that are worth understanding before selecting them for sensitive applications. - **Shear stress on biological products.** Roller compression creates localized shear forces each time the tubing is squeezed. Changes in speed, occlusion, or tubing geometry can amplify that stress. Live cells and fragile biomolecules are particularly vulnerable to shear-related damage during transfer. - **Tubing wear and particle shedding.** Continuous roller contact causes tubing abrasion and stretching over time. This wear can release microscopic particles — a phenomenon known as spallation — which can compromise product purity and create regulatory compliance issues. - **Variability in accuracy.** Flow rate changes as tubing fatigues. Pulsation increases at lower speeds, and repeatability can degrade significantly over long production runs. - **Operational downtime.** Tubing must be replaced and recalibrated regularly, adding time and cost to changeovers. ### i-FILL® vs. Peristaltic Pumps: At a Glance **Feature** **Peristaltic Pump** **i-FILL®** Flow mechanism Tubing compression Diaphragm displacement Shear risk Moderate to high Minimal Fill accuracy Variable High repeatability Pulsation Present Low to none Tubing wear Yes — routine replacement No mechanical wear Single-use fluid path Limited Standard Best for General transfer, low-value fluids Live cells, biologics, aseptic fill-finish ### When Is i‑FILL® the Better Choice? i‑FILL® is the stronger choice when you are handling live cells or shear-sensitive biologics, when precision and repeatability are critical, when product value justifies investment in accuracy, or when you need consistent performance over thousands of cycles with single-use fluid paths. It may not be the best fit when the application involves very high-viscosity fluids, precision requirements are low, or simple bulk transfer is the primary objective. In those cases, traditional peristaltic pumps remain a practical and cost-effective solution. ### Talk to Intellitech About Your Application Every process is different. Intellitech engineers work directly with customers to identify the most appropriate filling and pumping technology for each product and regulatory environment. If you are evaluating peristaltic pumps versus i‑FILL® technology, our team can assess your product sensitivity, volume range, accuracy requirements, and compliance needs. [Contact Intellitech](https://intellitech-inc.com/contact-us/) to discuss your specific application — or [request a quote](https://intellitech-inc.com/request-a-quote/) to get started. [ ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-fill-front-image1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-Oct-2023-4-scaled-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/2-days-MF-IF-1-Hour-BC-Adjusted-300x200-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/4-i-FILL-Cell-viability-after-2-hours-and-2-days.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/PrestoBlue-Assay-Picture.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6613.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2024/12/i-fill-micro-front-12-24.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6127.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6114.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6119.webp) Accurate, repeatable low‑volume dispensing is a critical challenge across life science process development, quality control laboratories, and fill/finish operations. Traditional pump technologies—peristaltic, syringe, and gear pumps—were largely designed for continuous flow rather than discrete microliter‑to‑milliliter fills. As fill volumes decrease and product value increases, variability, shear stress, and contamination risk become increasingly costly. This white paper presents a purpose‑built alternative: the i‑FILL® Micro single‑use dispensing system. Using a mechanically defined piston stroke and a closed, disposable fluid path, i‑FILL delivers highly repeatable µL–mL volumes with minimal shear and no cleaning validation burden. Performance data, application examples, and operational considerations are discussed to support evaluation by process engineers, lab technicians, scientists, and fill/finish supervisors. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### i‑FILL® Micro Technology Overview The i‑FILL Micro is a hybrid piston/diaphragm dispensing pump designed specifically for discrete, low‑volume fills. Unlike flow‑based systems, dispense volume is **defined mechanically**. #### Key Design Principles - **Digitally controlled piston stroke:** Each dispense cycle is determined by a fixed stroke length that does not change over time. - **Single‑use fluid path kits:** All wetted components—including tubing, check valves, and dispense tip—are disposable, eliminating cleaning validation and cross‑contamination risk. - **Closed‑loop fluid path:** Check valves support drip‑free operation and consistent delivery. - **Servo‑motor drive:** Ensures repeatable motion and stroke precision cycle after cycle. Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Single‑Use Kit Configurations and Fill Ranges Two single‑use kit sizes support a wide range of volumes in a single stroke: - 1 mL kit: approximately 350 µL to 1 mL - 10 mL kit: approximately 500 µL to 19 mL Extensive internal testing was performed to identify minimum and maximum volumes that maintain consistent volumetric accuracy across repeated dispenses. Reference charts in the operations manual correlate piston stroke distance (mm) with approximate dispense volume, simplifying setup and reducing guesswork. All kits are double‑bagged, gamma‑irradiated, supplied with material certifications and lot traceability, and have a two‑year shelf life. ### Volumetric Accuracy Performance Data To quantify repeatability, i‑FILL Micro was evaluated across minimum and maximum dispense limits for both kit sizes. Each data set represents 100 consecutive dispenses, providing insight into performance over time—not isolated measurements. #### 5.1 10 mL Kit Performance **Figure 1. Minimum Dispense – 10 mL Kit** Approximately 0.5 mL dispensed at a piston distance of ~5.76 mm over 100 trials. Results demonstrate ±2% volumetric accuracy with no widening of dispersion over time. **Figure 2. Maximum Dispense – 10 mL Kit** Approximately 19.3 mL dispensed at a piston distance of ~46 mm over 100 trials. Results maintain ±0.25% volumetric accuracy, indicating exceptional repeatability at the upper end of the kit’s range. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 10 mL Kit (27‑MAR‑2026)** These results highlight a key advantage over elastic tubing systems, which often show increased variability as runs progress. With i‑FILL, dispersion does not increase during operation. #### 5.2 1 mL Kit Performance **Figure 3. Minimum Dispense – 1 mL Kit** Approximately 350 µL dispensed at a piston distance of ~9.16 mm over 100 trials. Accuracy is maintained at ±2%, even at sub‑milliliter volumes. **Figure 4. Maximum Dispense – 1 mL Kit** Approximately 1.1 mL dispensed at a piston distance of ~18 mm over 100 trials. Accuracy tightens to ±0.25% across the data set. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 1 mL Kit (27‑MAR‑2026)** At volumes where many pump technologies struggle, the i‑FILL’s fixed mechanical stroke delivers predictable, repeatable performance without recalibration or operator intervention. ### Implications for Yield and Process Control For many processes, especially fill/finish of high‑value materials, accuracy improvements translate directly into recovered yield. Tight repeatability enables: - Reduced overfill safety margins - Higher confidence in batch‑to‑batch consistency - Less material lost to conservative process assumptions For process engineers, this opens opportunities to optimize specifications and improve overall process economics without compromising quality. ### Handling Shear‑Sensitive and Live Cell Applications Beyond accuracy, material integrity is often paramount—particularly for live cells and shear‑sensitive biologics. Peristaltic pumps generate localized shear through repeated tubing compression, which can negatively impact cell viability. The i‑FILL Micro was evaluated for live cell transfer in collaboration with the University of South Florida using recirculation protocols. #### Study Highlights - Comparative testing against well‑established peristaltic pumps - Multiple cell cultures evaluated - Two completed studies presented as posters at: - Advanced Therapies Week 2024 (Miami) - Multiple cell cultures evaluated - A third study currently in progress Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. **Figure 5. Microscopy Comparison** Cultured cells circulated for 5 minutes using i‑FILL versus peristaltic pumping show preserved morphology and viability when handled by i‑FILL. These results support the use of i‑FILL where cell viability, process confidence, and product protection are critical. ### Application Areas i‑FILL Micro is well suited for: - Biologics fill/finish - Cell therapy manufacturing and development - Media, buffer, and reagent dispensing - Transfer of viscous or shear‑sensitive fluids - R&D and pilot‑scale process development The system is not intended to replace every pump in a facility, but to complement existing technologies where precision and repeatability are essential. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### Implementation, Ordering, and Support Through Cole‑Parmer, users have access to a complete i‑FILL resource ecosystem: - Product selection and ordering via coleparmer.com - Quick start guides, operation manuals, and specification sheets - Demo and training resources - Global inventory and distribution - Technical guidance, integration, and troubleshooting support This infrastructure simplifies deployment from early adoption through scale‑up. As life science processes continue to move toward smaller volumes and higher‑value materials, the limitations of traditional dispensing technologies become more pronounced. By defining volume mechanically and eliminating variability associated with elastic components and reuse, the i‑FILL® Micro system offers a robust solution for precision µL–mL dispensing. **Categories:** Uncategorized --- ### [Precision Single‑Use Micro‑Volume Dispensing for Life Science Applications](https://intellitech-inc.com/precision-single-use-micro-volume-dispensing/) **Published:** April 16, 2026 **Author:** craig **Content:** Accurate, repeatable low‑volume dispensing is a critical challenge across life science process development, quality control laboratories, and fill/finish operations. Traditional pump technologies—peristaltic, syringe, and gear pumps—were largely designed for continuous flow rather than discrete microliter‑to‑milliliter fills. As fill volumes decrease and product value increases, variability, shear stress, and contamination risk become increasingly costly. This white paper presents a purpose‑built alternative: the i‑FILL® Micro single‑use dispensing system. Using a mechanically defined piston stroke and a closed, disposable fluid path, i‑FILL delivers highly repeatable µL–mL volumes with minimal shear and no cleaning validation burden. Performance data, application examples, and operational considerations are discussed to support evaluation by process engineers, lab technicians, scientists, and fill/finish supervisors. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### i‑FILL® Micro Technology Overview The [**i‑FILL Micro**](https://intellitech-inc.com/i-fill-micro/ "i-FILL Micro") is a hybrid piston/diaphragm dispensing pump designed specifically for discrete, low‑volume fills. Unlike flow‑based systems, dispense volume is **defined mechanically**. #### Key Design Principles - **Digitally controlled piston stroke:** Each dispense cycle is determined by a fixed stroke length that does not change over time. - **Single‑use fluid path kits:** All wetted components—including tubing, check valves, and dispense tip—are disposable, eliminating cleaning validation and cross‑contamination risk. - **Closed‑loop fluid path:** Check valves support drip‑free operation and consistent delivery. - **Servo‑motor drive:** Ensures repeatable motion and stroke precision cycle after cycle. Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. ![live cell transfer pump Cleanroom Assembly i-FILL i-FILL Micro](https://intellitech-inc.com/wp-content/uploads/2020/07/iFIll-Micro.png "iFIll-Micro - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ![.](https://intellitech-inc.com/wp-content/uploads/2026/04/validate-bkg-new-1024x301.jpg "validate-bkg-new - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Single‑Use Kit Configurations and Fill Ranges Two [**single‑use**](https://intellitech-inc.com/single-use-systems/ "Single-Use Systems") kit sizes support a wide range of volumes in a single stroke: - 1 mL kit: approximately 350 µL to 1 mL - 10 mL kit: approximately 500 µL to 19 mL Extensive internal testing was performed to identify minimum and maximum volumes that maintain consistent volumetric accuracy across repeated dispenses. Reference charts in the operations manual correlate piston stroke distance (mm) with approximate dispense volume, simplifying setup and reducing guesswork. All kits are double‑bagged, gamma‑irradiated, supplied with material certifications and lot traceability, and have a two‑year shelf life. ### Volumetric Accuracy Performance Data To quantify repeatability, i‑FILL Micro was evaluated across minimum and maximum dispense limits for both kit sizes. Each data set represents 100 consecutive dispenses, providing insight into performance over time—not isolated measurements. #### 5.1 10 mL Kit Performance **Figure 1. Minimum Dispense – 10 mL Kit** Approximately 0.5 mL dispensed at a piston distance of ~5.76 mm over 100 trials. Results demonstrate ±2% volumetric accuracy with no widening of dispersion over time. **Figure 2. Maximum Dispense – 10 mL Kit** Approximately 19.3 mL dispensed at a piston distance of ~46 mm over 100 trials. Results maintain ±0.25% volumetric accuracy, indicating exceptional repeatability at the upper end of the kit’s range. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 10 mL Kit (27‑MAR‑2026)** These results highlight a key advantage over elastic tubing systems, which often show increased variability as runs progress. With i‑FILL, dispersion does not increase during operation. #### 5.2 1 mL Kit Performance **Figure 3. Minimum Dispense – 1 mL Kit** Approximately 350 µL dispensed at a piston distance of ~9.16 mm over 100 trials. Accuracy is maintained at ±2%, even at sub‑milliliter volumes. **Figure 4. Maximum Dispense – 1 mL Kit** Approximately 1.1 mL dispensed at a piston distance of ~18 mm over 100 trials. Accuracy tightens to ±0.25% across the data set. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 1 mL Kit (27‑MAR‑2026)** At volumes where many pump technologies struggle, the i‑FILL’s fixed mechanical stroke delivers predictable, repeatable performance without recalibration or operator intervention. ### Implications for Yield and Process Control For many processes, especially fill/finish of high‑value materials, accuracy improvements translate directly into recovered yield. Tight repeatability enables: - Reduced overfill safety margins - Higher confidence in batch‑to‑batch consistency - Less material lost to conservative process assumptions For process engineers, this opens opportunities to optimize specifications and improve overall process economics without compromising quality. ### Handling Shear‑Sensitive and Live Cell Applications Beyond accuracy, material integrity is often paramount—particularly for live cells and shear‑sensitive biologics. Peristaltic pumps generate localized shear through repeated tubing compression, which can negatively impact cell viability. The i‑FILL Micro was evaluated for live cell transfer in collaboration with the University of South Florida using recirculation protocols. #### Study Highlights - Comparative testing against well‑established peristaltic pumps - Multiple cell cultures evaluated - Two completed studies presented as posters at: - Advanced Therapies Week 2024 (Miami) - Multiple cell cultures evaluated - A third study currently in progress Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. **Figure 5. Microscopy Comparison** Cultured cells circulated for 5 minutes using i‑FILL versus peristaltic pumping show preserved morphology and viability when handled by i‑FILL. These results support the use of i‑FILL where cell viability, process confidence, and product protection are critical. ### Application Areas [**i‑FILL Micro**](https://intellitech-inc.com/i-fill-micro/ "i-FILL Micro") is well suited for: - Biologics fill/finish - Cell therapy manufacturing and development - Media, buffer, and reagent dispensing - Transfer of viscous or shear‑sensitive fluids - R&D and pilot‑scale process development The system is not intended to replace every pump in a facility, but to complement existing technologies where precision and repeatability are essential. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### Implementation, Ordering, and Support Through [**Cole‑Parmer**](https://www.coleparmer.com/), users have access to a complete [**i‑FILL**](https://intellitech-inc.com/i-fill/ "i-FILL") resource ecosystem: - Product selection and ordering via coleparmer.com - Quick start guides, operation manuals, and specification sheets - Demo and training resources - Global inventory and distribution - Technical guidance, integration, and troubleshooting support This infrastructure simplifies deployment from early adoption through scale‑up. As life science processes continue to move toward smaller volumes and higher‑value materials, the limitations of traditional dispensing technologies become more pronounced. By defining volume mechanically and eliminating variability associated with elastic components and reuse, the i‑FILL® Micro system offers a robust solution for precision µL–mL dispensing. ### Achieve Reliable Micro-Volume Dispensing With Confidence When accuracy, repeatability, and product protection matter, Intellitech’s precision single-use dispensing solutions provide the control needed for demanding biopharmaceutical applications. From research and development through GMP production, the i-FILL® Micro helps streamline small-volume filling processes while minimizing product waste and simplifying fluid path management. Ready to improve your micro-volume dispensing process? **[Contact Intellitech to discuss your application](https://intellitech-inc.com/contact-us/ "Contact Us")**and find the right precision pumping solution. [ ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-fill-front-image1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-Oct-2023-4-scaled-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/2-days-MF-IF-1-Hour-BC-Adjusted-300x200-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/4-i-FILL-Cell-viability-after-2-hours-and-2-days.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/PrestoBlue-Assay-Picture.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6613.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2024/12/i-fill-micro-front-12-24.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6127.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6114.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6119.webp) Accurate, repeatable low‑volume dispensing is a critical challenge across life science process development, quality control laboratories, and fill/finish operations. Traditional pump technologies—peristaltic, syringe, and gear pumps—were largely designed for continuous flow rather than discrete microliter‑to‑milliliter fills. As fill volumes decrease and product value increases, variability, shear stress, and contamination risk become increasingly costly. This white paper presents a purpose‑built alternative: the i‑FILL® Micro single‑use dispensing system. Using a mechanically defined piston stroke and a closed, disposable fluid path, i‑FILL delivers highly repeatable µL–mL volumes with minimal shear and no cleaning validation burden. Performance data, application examples, and operational considerations are discussed to support evaluation by process engineers, lab technicians, scientists, and fill/finish supervisors. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### i‑FILL® Micro Technology Overview The i‑FILL Micro is a hybrid piston/diaphragm dispensing pump designed specifically for discrete, low‑volume fills. Unlike flow‑based systems, dispense volume is **defined mechanically**. #### Key Design Principles - **Digitally controlled piston stroke:** Each dispense cycle is determined by a fixed stroke length that does not change over time. - **Single‑use fluid path kits:** All wetted components—including tubing, check valves, and dispense tip—are disposable, eliminating cleaning validation and cross‑contamination risk. - **Closed‑loop fluid path:** Check valves support drip‑free operation and consistent delivery. - **Servo‑motor drive:** Ensures repeatable motion and stroke precision cycle after cycle. Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Operation and Workflow From installation to operation, i‑FILL is designed for simplicity and reproducibility: - **Install the single‑use kit** by aligning three mounting points and securing with thumb screws (no tools required). - **Power on and prime** to purge air and establish a stable fluid path. - **Load dispensing parameters** via recipe selection or manual entry. - **Dispense** using the touchscreen or a hands‑free foot switch for ergonomic operation. Once primed, volume consistency is governed by piston travel distance—not operator technique or material elasticity—resulting in highly repeatable fills over hundreds of cycles. ### Single‑Use Kit Configurations and Fill Ranges Two single‑use kit sizes support a wide range of volumes in a single stroke: - 1 mL kit: approximately 350 µL to 1 mL - 10 mL kit: approximately 500 µL to 19 mL Extensive internal testing was performed to identify minimum and maximum volumes that maintain consistent volumetric accuracy across repeated dispenses. Reference charts in the operations manual correlate piston stroke distance (mm) with approximate dispense volume, simplifying setup and reducing guesswork. All kits are double‑bagged, gamma‑irradiated, supplied with material certifications and lot traceability, and have a two‑year shelf life. ### Volumetric Accuracy Performance Data To quantify repeatability, i‑FILL Micro was evaluated across minimum and maximum dispense limits for both kit sizes. Each data set represents 100 consecutive dispenses, providing insight into performance over time—not isolated measurements. #### 5.1 10 mL Kit Performance **Figure 1. Minimum Dispense – 10 mL Kit** Approximately 0.5 mL dispensed at a piston distance of ~5.76 mm over 100 trials. Results demonstrate ±2% volumetric accuracy with no widening of dispersion over time. **Figure 2. Maximum Dispense – 10 mL Kit** Approximately 19.3 mL dispensed at a piston distance of ~46 mm over 100 trials. Results maintain ±0.25% volumetric accuracy, indicating exceptional repeatability at the upper end of the kit’s range. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 10 mL Kit (27‑MAR‑2026)** These results highlight a key advantage over elastic tubing systems, which often show increased variability as runs progress. With i‑FILL, dispersion does not increase during operation. #### 5.2 1 mL Kit Performance **Figure 3. Minimum Dispense – 1 mL Kit** Approximately 350 µL dispensed at a piston distance of ~9.16 mm over 100 trials. Accuracy is maintained at ±2%, even at sub‑milliliter volumes. **Figure 4. Maximum Dispense – 1 mL Kit** Approximately 1.1 mL dispensed at a piston distance of ~18 mm over 100 trials. Accuracy tightens to ±0.25% across the data set. **Insert: i‑FILL Micro Min and Max Dispense Data Charts – 1 mL Kit (27‑MAR‑2026)** At volumes where many pump technologies struggle, the i‑FILL’s fixed mechanical stroke delivers predictable, repeatable performance without recalibration or operator intervention. ### Implications for Yield and Process Control For many processes, especially fill/finish of high‑value materials, accuracy improvements translate directly into recovered yield. Tight repeatability enables: - Reduced overfill safety margins - Higher confidence in batch‑to‑batch consistency - Less material lost to conservative process assumptions For process engineers, this opens opportunities to optimize specifications and improve overall process economics without compromising quality. ### Handling Shear‑Sensitive and Live Cell Applications Beyond accuracy, material integrity is often paramount—particularly for live cells and shear‑sensitive biologics. Peristaltic pumps generate localized shear through repeated tubing compression, which can negatively impact cell viability. The i‑FILL Micro was evaluated for live cell transfer in collaboration with the University of South Florida using recirculation protocols. #### Study Highlights - Comparative testing against well‑established peristaltic pumps - Multiple cell cultures evaluated - Two completed studies presented as posters at: - Advanced Therapies Week 2024 (Miami) - Multiple cell cultures evaluated - A third study currently in progress Pump parameters are set and recalled through a touchscreen HMI using recipe‑based control. Operators can execute locked methods, while administrators manage access through password‑protected logins—supporting controlled laboratory and GMP environments. **Figure 5. Microscopy Comparison** Cultured cells circulated for 5 minutes using i‑FILL versus peristaltic pumping show preserved morphology and viability when handled by i‑FILL. These results support the use of i‑FILL where cell viability, process confidence, and product protection are critical. ### Application Areas i‑FILL Micro is well suited for: - Biologics fill/finish - Cell therapy manufacturing and development - Media, buffer, and reagent dispensing - Transfer of viscous or shear‑sensitive fluids - R&D and pilot‑scale process development The system is not intended to replace every pump in a facility, but to complement existing technologies where precision and repeatability are essential. ### The Challenge of Low‑Volume Dispensing The Challenge of In biologics, cell therapy, and advanced research environments, every microliter can represent significant time, cost, and risk. Common challenges encountered with conventional dispensing technologies include: - Accuracy drift over time due to tubing relaxation or mechanical wear - Operator‑to‑operator variability driven by manual adjustments - Shear sensitivity, particularly for live cells and fragile biomolecules - Contamination and carryover risk from reusable fluid paths - Overfilling safety margins that lead to unnecessary product loss As dispensing volumes move below 1 mL, small sources of variability are amplified. Systems that infer volume from flow are inherently sensitive to elastic components, tubing age, and fluid properties. These limitations motivate a fundamentally different approach to defining volume. ### Implementation, Ordering, and Support Through Cole‑Parmer, users have access to a complete i‑FILL resource ecosystem: - Product selection and ordering via coleparmer.com - Quick start guides, operation manuals, and specification sheets - Demo and training resources - Global inventory and distribution - Technical guidance, integration, and troubleshooting support This infrastructure simplifies deployment from early adoption through scale‑up. As life science processes continue to move toward smaller volumes and higher‑value materials, the limitations of traditional dispensing technologies become more pronounced. By defining volume mechanically and eliminating variability associated with elastic components and reuse, the i‑FILL® Micro system offers a robust solution for precision µL–mL dispensing. **Categories:** Uncategorized --- ### [Gentle Pumping You Can Trust for Cell Therapy Applications](https://intellitech-inc.com/gentle-pumping-you-can-trust-for-cell-therapy-applications/) **Published:** April 10, 2026 **Author:** craig **Content:** In cell and gene therapy manufacturing, protecting cell health is critical at every step. Fluidhandling systems must move cells reliably and efficiently—without introducing unnecessary stress that could impact viability or function. The **[iFILL™ Micro](https://intellitech-inc.com/i-fill-micro/ "i-FILL Micro")**Hybrid Piston Diaphragm (HPD) pump was developed with this challenge in mind. Unlike traditional peristaltic pumps that rely on repeated tubing compression, the iFILL™ Micro uses a precision controlled diaphragm inside a disposable fluid path. This approach maintains a closed, sterile system while eliminating continuous tubing deformation—offering a gentler way to move sensitive cells. To ensure this design performs where it matters most, Intellitech evaluated the iFILL™ Micro in a direct comparison study using primary **human T cells**, a clinically relevant and highly delicate cell type commonly used in cell therapy workflows. Cells were circulated through closed systems using either the iFILL™ Micro or a standard peristaltic pump under equivalent operating conditions. ### The Results: Cell Health Preserved The study showed that **cells pumped with the iFILL™ Micro remain healthy and functional**, performing on par with cells handled by traditional peristaltic pumps: - **High cell viability (>97%)** was maintained across all test conditions - **No delayed or hidden damage** was observed over a sevenday recovery period - **Normal cell morphology and integrity** were preserved throughout In short, the iFILL™ Micro demonstrated that it can safely handle fragile human T cells without compromising viability, recovery, or longer term cellular performance. ### Why It Matters These findings give manufacturers confidence that the iFILL™ Micro can be integrated into existing and nextgeneration cell therapy processes without introducing additional risk to valuable cell products. At the same time, its unique pumping mechanism offers meaningful advantages beyond cell safety, including: - Precise, repeatable fluid control - Reduced mechanical wear on disposable components - A robust alternative to traditional peristaltic pumping ### A Modern Option for Advanced Cell Manufacturing By combining proven cell viability with a differentiated fluidhandling approach, the **iFILL™ Micro pump** provides a reliable, forwardlooking solution for advanced cell and gene therapy workflows—supporting both today’s manufacturing needs and tomorrow’s innovations. ### Precision Matters When Handling Cellular Therapies From research and development to GMP production, Intellitech provides gentle, reliable pumping solutions designed to support the safe transfer of sensitive biological materials. Learn how the i-FILL® family of precision pumps can help protect cell viability while improving consistency and efficiency in your process. Ready to discuss your cell therapy application? **[Contact Intellitech today to explore a customized solution.](https://intellitech-inc.com/contact-us/ "Contact Us")** [ ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-fill-front-image1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-Oct-2023-4-scaled-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/2-days-MF-IF-1-Hour-BC-Adjusted-300x200-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/4-i-FILL-Cell-viability-after-2-hours-and-2-days.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/PrestoBlue-Assay-Picture.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6613.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2024/12/i-fill-micro-front-12-24.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6127.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6114.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6119.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2026/04/intellitech-ifill-image-3.webp) **Categories:** Uncategorized --- ## Pages ### [Home](https://intellitech-inc.com/) **Published:** May 14, 2025 **Author:** seouser **Content:** ##### Filling Tomorrow's Needs Today # Bioprocessing Integrated Solutions for Biopharma & Biotech (R&D to GMP) #### Custom Single Use Systems For Biopharma Manufacturing ### Custom Single Use Systems For Biopharma Intellitech has unique experience in the design, development and manufacture of many assemblies used in BIO/PHARMA development and production. [Learn More](/single-use-systems/) #### i-FILL Pumps For Precision Dispensing and Cell Transfer ### i-FILL Pumps For Precision Dispensing and Cell Transfer The i-FILL® delivers unmatched, repeatable dispense accuracy over thousands of dispenses for volumes up to 100mL, while also being qualified for live-cell transfer. [Learn More](https://intellitech-inc.com/products/#ifill-products) ## Custom Single Use Systems For Biopharma Intellitech has unique experience in the design, development and manufacture of many custom single use assemblies used in bioprocessing development and production. [ Learn More ](/single-use-systems/) ## i-FILL Pumps For Precision Dispensing and Cell Transfer The i-FILL® delivers unmatched, repeatable dispense accuracy over thousands of dispenses for volumes up to 100mL, while also being qualified for live-cell transfer in bioprocessing. [ Learn More ](https://intellitech-inc.com/products/#ifill-products) ## Explore Intellitech's Services #### Intellitech Covers The Spectrum To Support Customers From R&D To GMP. [![](https://intellitech-inc.com/wp-content/uploads/2024/11/design-engineering-icon.webp "design-engineering-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/design-engineering/)### [Design & Engineering Services](/design-engineering/) [ Learn More ](/design-engineering/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/prototyping-fabrication-icon.webp "prototyping-fabrication-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/prototyping-fabrication/)### [Prototyping & Fabrication Services](/prototyping-fabrication/) [ Learn More ](/prototyping-fabrication/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/assembly-packaging-icon.webp "assembly-packaging-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/cleanroom-assembly-packaging/)### [Cleanroom Assembly & Packaging Services](/cleanroom-assembly-packaging/) [ Learn More ](/cleanroom-assembly-packaging/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/testing-validation-icon.webp "testing-validation-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/testing-validation/)### [Testing & Validation Services](/testing-validation/) [ Learn More ](/testing-validation/) Product Design Prototype Testing / Validation #### Product Design Intellitech supports customers in the R&D phase to define, develop and document elements of the Design history file. - Requirements and Specification - Feasibility - Risk Analysis - Drawings [ More Details ](/services-rd/) #### Prototype Capability to deliver advanced product prototypes with 3D printing or development lab bench-built first articles. [ More Details ](/services-rd/#prototype) #### Testing / Validation Intellitech supports customers to validate processes and define acceptable operating ranges, critical quality attributes, and acceptance criteria of the intended system(s). [ More Details ](/services-gmp/) ## Our Quality Policy Intellitech, Inc is committed to satisfying biotech and biopharma customers through the on-time delivery of products that meet requirements while continuously improving the effectiveness of our Quality Management System. [ Learn More ](/our-quality-policy/) ## About Intellitech Intellitech manufactures the i-FILL® family of precision pumps and single use systems for bioprocessing for the biotechnology and pharmaceutical industries. Founded and operated by industry experts Andy and Barbara Biller, Intellitech is known for its commitment to on-time delivery of high-quality products to its customers. The Billers have built Intellitech on the principles of quality and innovation, creating a company that provides tailored solutions to meet the specific applications of manufacturers in the life science industry. Intellitech offers a range of services, primarily focused on designing, manufacturing, sterilizing, and validating disposable processing systems for biopharma. These single-use systems are custom-built and packaged in an ISO7-certified cleanroom environment. This ensures that these products are well integrated into our customers’ processes and that they meet the sterility requirements of drug/biologic manufacturers, supporting efficient bioprocess manufacturing. Among Intellitech’s core products are the i-FILL and the i-FILL Micro. These pumps are designed for high configurability, accuracy, and utilization of single-use components, ensuring compatibility for demanding bio/pharma dispensing or product transfer applications. The i-FILL pump is capable of handling a wide range of fill volumes, making it ideal for unit operations where consistency and versatility in flow rates are key. The i-FILL Micro is engineered for applications that require small-volume filling or transfer of sensitive or high value product. The pump and single use fluid path are qualified for live cell transfer with proven cell viability. Intellitech meets customer requirements with personalized support and tailored solutions, making them a trusted partner in the biotechnology and pharmaceutical industries, supporting advancements in biotech product development and efficient biopharma production process. [ Learn More ](/about/) ![.](https://intellitech-inc.com/wp-content/uploads/2025/06/intellitech-logo-icon-lg-2025.png "intellitech-logo-icon-lg-2025 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ## Precision Liquid Filling – Validated Accuracy ### Request a Quote ##### Innovative bioprocessing solutions that are custom configured to meet your needs. Contact us today to build a custom liquid filling machine with tighter fill tolerances to suit you. [ Request a quote ](/request-a-quote/) --- ### [Resources](https://intellitech-inc.com/resources/) **Published:** July 27, 2026 **Author:** shannon **Content:** # Resources ## Discover Our Custom Solutions ### Find Innovative Solutions With Us Intellitech specializes in designing and manufacturing custom single-use systems for the biopharmaceutical industry. If you can’t find a solution that fits your needs, we’re here to help. Our team works closely with you to bring your design concept from an initial sketch to a fully GMP-compliant product, ensuring the highest standards for quality and performance. ![.](https://intellitech-inc.com/wp-content/uploads/2025/06/intellitech-logo-stacked-2025.png "intellitech-logo-stacked-2025 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ## Frequently Asked Questions ## Questions & Answers From Our Recent Webinars #### What is the i‑FILL® pump accuracy? Pump accuracy depends on the kit size and dispensing volume. For both the 1 mL and 10 mL kits, accuracy is specified at ±2% at the lower end of the defined operating range. Within the mid-to-upper range of each kit, performance improves significantly — achieving ±0.25% accuracy across continuous runs of 100 dispenses. As a practical example, the 10 mL kit demonstrated ±2% accuracy at volumes as low as approximately 0.5 mL, while accuracy tightened to ±0.25% at mid and higher volumes (up to ~19.3 mL). Testing was performed using water-like fluids with no special temperature controls, and results reflect consistent, repeatable performance over hundreds of dispenses — not single-point claims. #### How is cell viability measured after passing through the i‑FILL® pump? Cell viability was evaluated using multiple protocols and time-based studies, including circulation periods of 5 minutes, 15 minutes, 2 hours, and up to 2 days. Established assays such as Trypan Blue staining were used throughout. Initial studies focused on basic viability — determining whether cells survived the transfer. Ongoing studies go further, assessing metabolic health and whether cells remain capable of replication and growth after processing. Each study follows a defined protocol, and summary results are available upon request from the Intellitech team. #### How easy is it to prime the i‑FILL® pump? Priming is designed to be fast and straightforward. The user mounts the appropriate single-use kit and selects a predefined priming recipe based on kit size. After placing the intake tubing into the source container, priming is initiated with the push of a button. Within three to four dispenses, air is fully expelled from the tubing set and the system is ready for operation. There are no complex tubing paths or manual adjustments required. #### Does the i‑FILL® pump require specialty tubing? No specialty tubing is required. Standard kits use platinum-cured silicone tubing, supported by full material certifications. If a different tubing material, length, or configuration is needed for a specific application, customization options are available through Intellitech. Users can select tubing that meets their process or regulatory requirements without relying on proprietary or uncommon materials. [Contact Intellitech](https://intellitech-inc.com/contact-us/) to discuss custom kit configurations for your application. ## ISO9001:2015 Certificate of Registration ### [Fill out our Contact Information form before downloading any documents below.](/contact-us/) ## Resource Documents ### Complete the Contact Form below to access our Documents. EmailThis field is for validation purposes and should be left unchanged. 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[ M1-022910 Tubing Weight for 0250 Tubing ](#) [ M1-03030 Tubing Weight for 0375 Tubing ](#) [ M1-03031 Tubing Weight for 0500 Tubing ](#) [ M1-03320 Tubing Weight for 0125 Tubing ](#) ### i-Fill Operation Manuals [ i-FILL Micro Operation Manual ](#) [ i-FILL Operation Manual ](#) ### i-Fill Warranty Information [ i-FILL Warranty Document ](#) ### Validation Summaries [ Validation Summaries & Doc Go Here ](#) ### Testing and Study Reports [ TR-2023-001 Pump Comparison Study 1 - Full Report ](#) [ TR-2023-001 Pump Comparison Study 2 - Full Report ](#) ## Resource Documents ### [Fill out our Contact Information form before downloading any documents below.](/contact-us/) ISO9001:2015 Certificate Quality Statements Specification Sheets i-Fill Operation Manuals i-Fill Warranty Information Validation Summaries Testing and Study Reports [ISO9001:2015 Certificate](https://intellitech-inc.com/wp-content/uploads/2022/12/Intellitech-NQA-ISO-9001-Certificate-18396_12-9-22.pdf) Tab Item Content [i-FILL Micro Specification Sheet](https://intellitech-inc.com/wp-content/uploads/2024/11/i-FILL-Micro-Technical-Specifications-Rev-4-31OCT2024.pdf) [i-FILL Specification Sheet](https://intellitech-inc.com/wp-content/uploads/2024/11/i-FILL-Technical-Specifications-Rev-4-31OCT2024.pdf) Tab Item Content Tab Item Content Tab Item Content Tab Item Content ## Resource Documents ### [Fill out our Contact Information form before downloading any documents below.](/contact-us/) ISO9001:2015 Certificate [ISO9001:2015 Certificate](https://intellitech-inc.com/wp-content/uploads/2022/12/Intellitech-NQA-ISO-9001-Certificate-18396_12-9-22.pdf) Quality Statements Accordion Item Content Specification Sheets [i-FILL Micro Specification Sheet](https://intellitech-inc.com/wp-content/uploads/2024/11/i-FILL-Micro-Technical-Specifications-Rev-4-31OCT2024.pdf) [i-FILL Specification Sheet](https://intellitech-inc.com/wp-content/uploads/2024/11/i-FILL-Technical-Specifications-Rev-4-31OCT2024.pdf) i-Fill Operation Manuals Accordion Item Content i-Fill Warranty Information Operation Manuals Accordion Item Content Validation Summaries Accordion Item Content Testing and Study Reports Accordion Item Content ### We welcome the opportunity to work with you ##### We support companies spanning the realm of R&D to GMP with a range of products and services. Call **1-727-914-7000** or [**contact us**](/contact-us/) to share your project, goals, and challenges. [ Contact Us ](/contact-us/) --- ### [i-FILL](https://intellitech-inc.com/i-fill/) **Published:** July 27, 2026 **Author:** shannon **Content:** # i-FILL #### Accurate and Repeatable Large Volume Filling ## i-FILL - Large Volume Filling The i-FILL® is a hybrid piston/diaphragm pump that delivers repeatable dispense accuracy for larger fill volumes up to 100mL per piston stroke. This larger volume is ideal for quick product transfer. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/i-FILL-image-cutout.webp "i-FILL-image-cutout - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### The i-FILL Offers - Semi-automated R&D, Lab, or Production Filling - Fill volumes up to 100mL per stroke - No tubing spallation - Multiple dispensing and flow rate profiles that can be stored as recipes - Ease of operation with its user-friendly interface - Reduce CIP/SIP Protocols with a Single-Use Pump Head [ Contact Us About The i-FILL ](/contact-us/) #### Contact Us to Learn More About the i-FILL Micro [ Contact Us ](/contact-us/) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/i-Fill-Product.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/i-FILL-interface-closeup.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6227.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6159.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6167.webp) ![](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-interface-1024x745.webp "I-FILL-interface - Intellitech Inc | Innovators of Single-Use Liquid Filling") #### A user-friendly interface allows users to easily adjust fill volumes, fill speeds, and flow rates. These settings can be saved into recipes to fit specific unit operations. [ i-FILL Spec Sheet ](/resources/) #### Intellitech collaborated with University of South Florida to study the i-FILL pump and a leading peristaltic pump for cell viability. 2 studies have been conducted to examine the application of the i-FILL Micro pumps for transporting live cells. The team conducted Trypan-blue cell viability experiments with sample volume suspensions. In the first study, NIH-3t3 mouse fibroblast cells were used. In the second study, human donor T-cells were used. In both studies, the cells were examined via live-cell imaging. The 2nd study also utilized Presto-blue assays as another method for measuring cell viability. In both studies, the results showed that the i-FILL Micro is capable for cell culture conditions during development and production. It is now qualified to be a viable alternative to the peristaltic pump. While the i-FILL pump has performed purely as a highly accurate dispensing pump, it is not proven to be a highly capable cell transfer pump for both upstream and downstream cell culturing and bioprocessing, e.g. product transfer from a mixing vessel to filtration, from filtration to cell harvesting and transfer to either a finishing or a storage vessel. ## Frequently Asked Questions on the i-FILL® Pump #### What is the pump accuracy? Pump accuracy depends on dispensing volume. For both the 1 mL and 10 mL kits, the largest volumetric accuracy is specified at ±2% for the lower end of the defined operating range. Within the mid-to-upper range of each kit, performance improves significantly, achieving ±0.25% accuracy across continuous runs of hundreds or thousands of dispenses. For example, the 10 mL kit demonstrated ±2% accuracy at volumes as low as approximately 0.3 mL, while accuracy tightened to ±0.25% at mid and higher volumes (1ml to 19 mL). Testing was performed using water-like fluids, with no special temperature controls, and results reflect consistent, repeatable performance over hundreds of dispenses rather than single-point claims. #### How easy is it to prime the pump? Priming the pump is designed to be straightforward and quick. The user mounts the appropriate single-use kit and selects a predefined priming recipe based on kit size. After placing the intake tubing into the source container, the user initiates priming with the push of a button. Within three to four dispenses, the pump is primed such that air is expelled from the tubing set and the system is ready for operation. The process does not involve complex tubing paths or manual adjustments. #### Is the pump compliant to 21 CFR 11? The pump supports key elements required for 21 CFR Part 11 compliance, including user access controls. Users must log in to modify pump parameters, ensuring controlled access to configuration settings. Operators can run pre-configured recipes without altering parameters, while administrative changes require appropriate credentials. These features support regulated environments where electronic access control and traceability are required. #### Can the pump be validated? Yes. The pump can be validated, and it is currently used in validated environments by existing customers. Validation protocols are available and align with the performance testing demonstrated during the webinar. Validation typically involves identifying the pump, recording operating parameters, running samples, and measuring dispensing results over time to confirm repeatability and consistency. #### Does the pump need to be calibrated? The pump itself does not require routine calibration or annual factory recalibration. However, best practice is to perform a benchmarking step for each new single-use kit. After priming, users are encouraged to run the pump onto a balance and verify the dispense volume. If needed, piston stroke length can be adjusted to fine-tune the volume. Once this initial adjustment is made, the kit can be considered set for use. This process accounts for minor kit-to-kit variability and ensures target volumes are met. #### Does the pump require specialty tubing? No specialty tubing is required. Standard kits use platinum-cured silicone tubing, supported by material certifications. However, kits can be customized if a different material, length, or configuration is required for a specific application, examples include tubing weights, fill bells, etc. Customization options are available, allowing users to select tubing that meets their process or regulatory needs without requiring proprietary or uncommon materials. #### Interested in learning more? Please provide your contact information. Name(Required) First Last Email(Required) Your Business Name(Required) Your Business Website Message(Required) CAPTCHA Submit ## Intellitech Products Many of our customers are involved in biologic drug/therapy/vaccine R&D and transitioning to GMP production and we, at Intellitech, believe we can best support those efforts by continuing to focus on manufacturing and improving the i-FILL family of precision liquid dispensing pump technology and single-use systems. #### Single Use Assemblies ### Single Use Assemblies Intellitech has unique experience in the design, development and manufacture of many assemblies used in BIO/PHARMA development and production. [Read More](https://intellitech-inc.com/single-use-assemblies/) #### Fluid/Cell Transfer Pump ### Fluid/Cell Transfer Pump The i-Fill® pump is proven effective to transfer live cells with little to no effect on the cells after varying tested periods of time. [Read More](https://intellitech-inc.com/fluid-cell-transfer-pump/) #### Precision Filling Pump ### Precision Filling Pump The i-Fill® delivers unmatched, repeatable dispense accuracy over thousands of dispenses for volumes of 100mcL to 100mL. [Read More](https://intellitech-inc.com/precision-filling-pump/) --- ### [Single-Use Systems](https://intellitech-inc.com/single-use-systems/) **Published:** June 12, 2026 **Author:** seouser **Content:** # Single-Use Systems ## ### Innovative Single-Use Systems for BIO/PHARMA R&D to GMP Single-Use Assemblies have various applications in biopharmaceutical development production such as cell culturing, sampling, mixing, filtration, and fill/finish. According to a survey by BioPlan Associates, over 85% of biopharmaceutical manufacturers use single-use systems in their production process. This effectively eliminates the high energy cost of clean-in-place/sterilization-in-place (CIP/SIP) protocols, resulting in improvements in sustainability. ### Bag Assemblies Bioprocessing bag assemblies play a crucial role in the development of biologic and pharmaceutical drug products. In bioprocessing, these bags are often used for bioprocessing applications such as product mixing, collection, storage, transfer, or transport. Bag materials are made to hold biologics, media, and other materials. Intellitech can offer these bags in 2D and 3D configurations and customize fittings and tubing to meet the requirements of a specific application. ![EGMO 2D single use bag assemblies  ](https://intellitech-inc.com/wp-content/uploads/2023/02/Bag-2-683x1024.png "Bag 2 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ![tubing sets](https://intellitech-inc.com/wp-content/uploads/2021/04/custom-samples-new2.png "custom-samples-new2 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Bottle Assemblies Similar to bioprocessing bags, sterile bottles are also important in biologic production. These containers are made for use in product mixing, sampling, storage, transport, bioreactors, and more. These bottles are also made to handle biopharmaceuticals as well as other bioprocess materials. Intellitech collaborates with its customers to determine the appropriate bottle size, material, and closure configuration to meet the requirements of their application. ### Request a Quote ##### Innovative solutions that are custom configured to meet your needs. Contact us today to build a custom single-use system that meets your requirements. [ Request a Quote ](/request-a-quote/) ### Filters Filters play a critical role in bioprocessing applications. They ensure that biological process fluids are sterile and that consistent pressure conditions remain in the processing tank or fluid path. Intellitech can supply these filters and incorporate them into designs according to our customer’s application and requirements. ### Mixing & Sampling “Experience seamless precision and unparalleled control in your bio/pharma operations with our cutting-edge needle assemblies and tubing connectors. **Mixing Excellence:** Our needle assemblies are engineered to deliver precision in transferring vital components during pharmaceutical formulation and bioprocessing. Ensure consistent dosages and homogeneous blends with our reliable assemblies, optimizing your mixing processes for superior product quality. **Seamless Sampling:** Elevate your quality control with our needle assemblies designed for precise and representative sample extraction. Coupled with our high-quality tubing connectors, seamlessly direct samples between instruments and testing points. Ensure accuracy and maintain the integrity of your analyses, adhering to the highest standards in sampling protocols. From ensuring uniformity in mixtures to maintaining the fidelity of your sampling procedures, our needle assemblies and tubing connectors are the backbone of reliability and precision in bio/pharma operations. Partner with us to elevate your processes and guarantee the quality and consistency of your pharmaceutical products.” ### Tubing Fittings and Connectors Choosing the right tubing fittings and connectors are critical for fluid management in bioprocessing applications. Sizing and materials must be carefully chosen to ensure proper fluid flow, sterility, and reduce the risk of leaks. Intellitech can offer many different fittings and connectors to meet the requirements of our customers. These parts also feature animal-derivative-free materials and meet USP Class VI requirements, both of which are important requirements for biopharmaceutical manufacturing. ### Filling Needle Assemblies Filling needle assemblies are vital in bio/pharma development, comprising a needle, hub, and sometimes a guard/sheath. Filling needle assemblies by Intellitech expertly facilitate precise liquid transfer while maintaining sterility. Intellitech can offer filling needles that come in many different configurations. For filling operations that are large or small, we work with our customers to meet their process requirements. ### Request a Quote ##### Innovative solutions that are custom configured to meet your needs. Contact us today to build a custom liquid filling machine with tighter fill tolerances to suit you. [ Request a quote ](/request-a-quote/) #### Interested in learning more? Please provide your contact information. Name(Required) First Last Email(Required) Your Business Name(Required) Your Business Website Message(Required) CAPTCHA Submit ## Intellitech Products Many of our customers are involved in biologic drug/therapy/vaccine R&D and transitioning to GMP production and we, at Intellitech, believe we can best support those efforts by continuing to focus on manufacturing and improving the i-FILL family of precision liquid dispensing pump technology and single-use systems. #### Single Use Assemblies ### Single Use Assemblies Intellitech has unique experience in the design, development and manufacture of many assemblies used in BIO/PHARMA development and production. [Read More](https://intellitech-inc.com/single-use-assemblies/) #### Fluid/Cell Transfer Pump ### Fluid/Cell Transfer Pump The i-Fill® pump is proven effective to transfer live cells with little to no effect on the cells after varying tested periods of time. [Read More](https://intellitech-inc.com/fluid-cell-transfer-pump/) #### Precision Filling Pump ### Precision Filling Pump The i-Fill® delivers unmatched, repeatable dispense accuracy over thousands of dispenses for volumes of 100mcL to 100mL. [Read More](https://intellitech-inc.com/precision-filling-pump/) --- ### [Terms & Conditions](https://intellitech-inc.com/terms-conditions/) **Published:** May 13, 2021 **Author:** craig **Content:** # Terms & Conditions THESE TERMS AND CONDITIONS OF SALE (THIS “AGREEMENT”) APPLY TO ALL QUOTATIONS, PURCHASE ORDERS, ACKNOWLEDGMENTS AND OFFERS FOR PRODUCTS ISSUED OR RECEIVED BY INTELLITECH, INC. (the “MANUFACTURER”) TO OR FROM CUSTOMER (“CUSTOMER”). MANUFACTURER’S ACCEPTANCE OF ANY CUSTOMER PURCHASE ORDER IS EXPRESSLY CONDITIONED ON CUSTOMER’S ASSENT TO THIS AGREEMENT. NO TERMS OR CONDITIONS SET FORTH IN CUSTOMER’S PURCHASE ORDER, TO WHICH NOTICE OF OBJECTION IS HEREBY GIVEN, OR IN ANY FUTURE CORRESPONDENCE BETWEEN CUSTOMER AND MANUFACTURER, SHALL ALTER OR SUPPLEMENT THIS AGREEMENT UNLESS BOTH PARTIES HAVE AGREED IN WRITING TO MODIFY THIS AGREEMENT. NEITHER MANUFACTURER’S COMMENCEMENT OF PERFORMANCE NOR DELIVERY OF ANY PRODUCT(S) SHALL BE DEEMED OR CON- STRUED AS ACCEPTANCE OF CUSTOMER’S ADDITIONAL OR DIFFERENT TERMS AND CONDITIONS. MANUFACTURER RESERVES THE RIGHT TO REJECT ANY ORDER OR TO CANCEL ANY ORDER PREVIOUSLY ACCEPTED IF MANUFACTURER DETERMINES THAT CUSTOMER IS IN BREACH OF ANY TERM OR CONDITION HEREIN. NOTWITHSTANDING THE FOREGOING, IN THE EVENT CUSTOMER AND MANUFACTURER HAVE A WRITTEN MANUFACTURE AND EQUIPMENT SALES AGREEMENT, THE TERMS OF SUCH AGREEMENT SHALL FURTHER SUPPLEMENT THESE TERMS. IN THE EVENT OF ANY CONFLICT OR INCONSISTENCY BETWEEN THE PROVISIONS OF A MANUFACTURE AND EQUIPMENT SALES AGREEMENT AND THESE STANDARD TERMS AND CONDITIONS OF SALE, THE CONFLICTING PROVISION OF THE MANUFACTURE AND EQUIPMENT SALE AGREEMENT SHALL CONTROL AND GOVERN. ### 1. PRICES. All quotations are in $US and shall constitute offers subject to this Agreement. Unless otherwise stated in writing by Manufacturer, all prices quoted: (i) expire thirty (30) days after the date they are provided to Customer; and (ii) are exclusive of transportation, insurance, federal, state, local, excise, value-added, use, sales, property (ad valorem) and similar taxes or duties now in force or hereafter in effect. In addition to the prices quoted or invoiced, Customer agrees to pay all taxes, fees, or charges of any nature whatsoever imposed by any governmental authority on, or measured by, the transaction between Customer and Manufacturer. If Manufacturer is required to collect such taxes, fees, or charges, such amounts will appear as separate items on Manufacturer’s invoice and will be paid by Customer. ### 2. TERMS OF PAYMENT. All invoices shall be paid in full in U.S. dollars within thirty (30) days of the invoice date unless payment terms are otherwise quoted. Customer shall pay a late fee of 1.5% per month. Manufacturer reserves the right at any time and for any reason to require payment in advance or COD, or to otherwise modify, suspend, or terminate any credit terms previously extended to Customer. If Manufacturer believes in good faith that Customer’s ability to make any payment required hereunder is or may be impaired, Manufacturer may cancel this Agreement (or any remaining balance thereof), and Customer shall remain liable to pay for any Product(s) previously shipped. When partial shipments are made, payments shall become due in accordance with the designated terms upon submission of an invoice covering any such partial shipment. ### 3. SHIPMENTS. In the absence of specific shipping instructions separately agreed to and set forth in a writing signed by both Parties, Manufacturer shall select a carrier who shall be deemed to act as Customer’s agent. Manufacturer shall be under no obligation to ship via any carrier selected by Customer if such carrier does not comply with applicable laws. Transportation charges will be collected on delivery or, if prepaid, will be subsequently invoiced to Customer. Unless otherwise indicated, Customer is obligated to obtain insurance against damage to Product(s) being shipped, and all Product(s) will be shipped in standard commercial packaging. When special or export packaging is requested or, in the opinion of Manufacturer, required under the circumstances, the cost of the same, if not set forth on the invoice, will be separately invoiced. All shipping dates are approximate, and Manufacturer may change the delivery date without penalty provided Manufacturer provides Customer with reasonable notice of such change. Manufacturer shall not be responsible for any failure to perform or delay in performing under this Agreement which is directly or indirectly due to circumstances beyond its reasonable control, including, without limitation, earthquakes, governmental regulation, fire, flood, labor difficulties, civil disorder, and acts of God. ### 4. ACCEPTANCE. Except as otherwise agreed in a writing signed by the Parties, Customer shall accept or reject Product(s) within thirty (30) days of receipt of each shipment. Failure to notify Manufacturer in writing of nonconforming Product(s) within such period shall be deemed an unqualified acceptance. ### 5. RETURN PROCEDURE. **PRODUCT(S) MAY NOT BE RETURNED IF IT IS NON-STANDARD, MADE-TO-ORDER, OR MANUFACTURED TO CUSTOMER’S SPECIFIC DESIGN OR SPECIFICATION, OR IS OUTDATED OR PHASE-OUT STOCK PRODUCT.** #### (a) Return Authorization Required. To obtain approval to return Product(s) to Manufacturer, Customer must contact Manufacturer’s Customer Service staff at 1- 866-434-5548, Monday through Friday, between the hours of 8 a.m. and 4:30 p.m. Eastern Standard Time (EST) or e-mail Customer Service at quality@intellitech-inc.com. If a return is approved, the Customer will receive a Return Material Authorization (“RMA”) form; a copy of which should be included with the return shipment. **NO PRODUCT RETURNS WILL BE ACCEPTED BY MANUFACTURER IF NOT ACCOMPANIED BY A VALID RMA.** Product(s) without an RMA number will either be refused or returned to Customer at Customer’s expense. Manufacturer is not liable for loss or damage to unauthorized Product(s) returns. Except for issues covered under these Terms and Conditions, all RMA requests must be made within 30 days of the invoice date to be eligible to receive credit. Once issued, RMA numbers are valid for 30 days. Any returns received after 30 days will be refused. Customer is responsible for all return freight charges, including taxes, customs, and duties if applicable. All Product(s) returned for credit must be new, undamaged, and in factory sealed packaging. Any Product(s) returned with marked box, damaged box, missing components, (e.g. cables, manuals, etc.), or other damage not caused by Manufacturer will be assessed a restocking fee premium to cover the cost of replacements. #### (b) Defective Product(s). Product(s) which Customer believes to be defective and covered by Manufacturer’s Limited Warranty (“Defective Product”) must be returned by Customer in accordance with the Return Procedure outlined above. Returned Product will be tested upon arrival at Manufacturer. Any Product(s) that is/are determined to be non-defective will be returned to Customer, at Customer’s expense, and a testing fee of a minimum of 10% of the Product(s) value will be assessed. If, following examination, Manufacturer determines to its satisfaction that such Product(s) is/are defective; Manufacturer will, at its option, repair or replace the Product(s) or the defective part thereof, or credit Customer for the purchase price therefore, subject to these Standard Terms and Conditions of Sale. For purposes of clarity, “repair or replace the Product(s) or the defective part thereof” does not include any removal or reinstallation costs or expenses, including without limitation labor costs or expenses. If Manufacturer chooses to replace the Product(s) and is not able to do so because it has been discontinued or is not available, Manufacturer may replace it with a comparable product. Manufacturer will cover standard ground shipping charges incurred by Purchaser for the return of defective Product(s) and the shipment of replacement Product(s). #### (c) Restocking Fees. Returns authorized by Manufacturer, other than return of defective Product(s), will be subject to a restocking fee and Customer will pay all transportation costs associated with the return, including taxes, customs, and duties, if applicable. Product(s) returned in original condition will be assessed a 25% restocking fee. If Product(s) is/are found to be dam- aged, missing manuals or parts, or if original Manufacturer’s carton is damaged or missing, a minimum 30% restocking fee will be charged. ### 6. DEFAULT, CANCELLATION, AND RESCHEDULING. In the event of Customer’s default in payment for the Product(s) purchased hereunder, Customer shall be responsible for all reasonable costs and expenses incurred by Manufacturer in collection of any sums owing by Customer (including reasonable attorneys’ fees), and Manufacturer may decline to make further shipments to Customer without in any way affecting its rights under this Agreement. If, despite any such breach by Customer, Manufacturer elects to continue to make shipments, such shipments shall not constitute a waiver of any breach by Customer or in any way affect Manufacturer’s legal remedies arising from such breach. ### 7. SECURITY INTEREST. Manufacturer hereby reserves for itself a purchase money security interest in all Product(s) sold hereunder and the proceeds thereof, in the amount of the purchase price. In the event of default by Customer in any of its obligations to Manufacturer, Manufacturer will have the right to repossess the Product(s) sold hereunder without liability to Customer. Such security interest will be satisfied by payment in full. A copy of the invoice may be filed with appropriate authorities at any time as a financing statement and/or chattel mortgage to perfect Manufacturer’s security interest. Upon request, Customer will execute such financing statements and other instruments as Manufacturer may request to perfect Manufacturer’s security interest herein. ### 8. DELIVERY AND TITLE. (a) Manufacturer shall select a carrier who shall be deemed to act as Customer’s agent. Manufacturer shall be under no obligation to ship via any carrier selected by Customer if such carrier does not comply with applicable laws. Transportation charges will be collected on delivery or, if prepaid, will be subsequently invoiced to Customer. Unless otherwise indicated, Customer is obligated to obtain insurance against damage to Product(s) being shipped, and all Product(s) will be shipped in standard commercial packaging. When special or export packaging is requested or, in the opinion of Manufacturer, required under the circumstances, the cost of the same, if not set forth on the invoice, will be separately invoiced. All shipping dates are approximate, and Manufacturer may change the delivery date without penalty provided Manufacturer provides Customer with reasonable notice of such change. (b) Title to the Product(s) and risk of loss or damage to the Product(s) shall pass to Customer at the Product’s manufacturing location, immediately upon delivery to a suitable carrier, subject to Manufacturer’s security interest in such Product(s) as described below. Notwithstanding title to the Product(s) passing to Customer, title shall not pass to Customer as to any Manufacturer intellectual property rights or Manufacturer software. ### 9. LIMITED WARRANTY. (a) Manufacturer warrants for a period of 6 months from the date of delivery (the “Warranty Period”) that Product(s) (except any excluded software) purchased and sold hereunder will substantially conform to Manufacturer’s published specifications or such other specifications specifically set forth in a separately negotiated and executed Manufacture and Equipment Sales Agreement. Repaired or replacement Product(s) provided under warranty are warranted for a period of 6 months from the date of delivery. The warranty on components not manufactured by Manufacturer, but incorporated as part of any system, is limited to the warranty provided by the original manufacturer of said components to the extent, and only to the extent, that such original manufacturer honors such warranty. Notwithstanding the foregoing, Manufacturer’s Product(s) are not designed, and no warranty is made with respect to Product(s) used in devices intended for use in applications where failure to perform when properly used can reasonably be expected to result in significant injury (including, without limitation, military or space applications, navigation, aviation, nuclear equipment, firefighting, or rescue equipment, or for surgical implant or to support or sustain life). Customer hereby represents and warrants to Manufacturer that it will not use or sell any Product(s) for any of the foregoing purposes and Customer agrees to indemnify, defend, and hold Manufacturer harmless from all claims, damages and liabilities arising out of any such uses. This limited warranty is contingent upon proper use of the Product(s) in the applications for which they were intended and does not apply to any Product(s) that are subjected to unusual physical or electrical stress, misuse, neglect, accident or which have been altered or soldered such that they are not capable of being tested under normal test conditions, improper testing or storage, unauthorized repair, or problems that arise from any use of Manufacturer’s Product(s) with other Product(s) not approved by Manufacturer. This limited warranty does not include expendable components. This limited warranty is nontransferable and shall extend only to Customer, and not to any third parties (including, without limitation, Customer’s suppliers, customers, or any end users). (b) This limited warranty is immediately voided by any design changes or modifications performed by anyone other than Manufacturer. (c) This limited warranty is immediately voided if any software incorporated into the Product(s) is altered or modified by anyone other than Manufacturer. (d) In the event of a breach of this limited warranty, Customer shall notify Manufacturer in writing by describing the nature of the non-conformity and return such Product(s) to Manufacturer in accordance with Company’s then current returned material authorization policies, within the Warranty Period. Customer shall ship such Product(s) back to Manufacturer at Customer’s expense. Manufacturer shall, at its option, promptly repair or replace non-conforming Product(s), or issue a credit for the purchase price of the nonconforming Product(s), and shall pay the costs of any such repair or replacement, including transportation costs incurred in returning repaired or replaced Product(s) to Customer unless (i) the Product(s) is/are not defective, in which case Customer shall pay Company reasonable costs of inspection and all transportation charges, or (ii) the Product(s) is/are defective due to Customer’s or any third party’s improper installation, repair, damage, misuse, abuse, or failure to use replacement parts and materials equivalent to Company’s parts and materials, in which case Customer shall pay all costs of repair or replacement and transportation. The remedy stated in these Terms and Conditions shall be Customer’s sole remedy in case of any breach of limited warranty by Manufacturer. (e) EXCEPT AS EXPRESSLY STATED IN THIS AGREEMENT AND TO THE MAXIMUM EXTENT PERMITTED BY APPLICABLE LAW, MANUFACTURER DISCLAIMS AND MAKES NO WARRANTIES. ALL PRODUCT(S) ARE PROVIDED AS IS, AS AVAILABLE, AND WITH ALL FAULTS, AND MANUFACTURER EXPRESSLY DISCLAIMS ALL OTHER WARRANTIES, EXPRESS, STATUTORY, OR IMPLIED, INCLUDING WITHOUT LIMITATION THE IMPLIED WARRANTIES OF NON-INFRINGEMENT, MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, OR ARISING OUT OF A COURSE OF DEALING TO THE MAXIMUM EXTENT PERMITTED BY LAW. ### 10. INDEMNITY. #### (a) Customer Indemnity. Customer shall indemnify, defend and hold Manufacturer harmless from and against any and all claims brought by any third party against Manufacturer arising out of or related to Customer’s use of the Product(s) purchased hereunder, including (i) any claim arising out of or related to any warranty made by or on behalf of Customer to its customers that expands any warranties provided herein or fails to limit any liability as provided herein, (ii) any claim arising out of Customer’s failure to secure all ownership or rights/permissions that convey to Intellitech the lawful right to design, copy and/or modify product design data inputs, or samples, provided to Intellitech, or (iii) any breach of this Agreement by Customer; provided, Manufacturer: a. gives prompt written notice to Customer of the institution of the suit or proceedings; and b. permits Customer through its counsel to defend the same and gives Customer all needed information, assistance and authority to enable Customer to do so. #### (b) Company Indemnity. Subject to the limitations herein, Manufacturer shall defend any suit or proceeding brought against Customer if it is based on a claim that any Product(s) furnished hereunder constitutes an infringement of any third-party copyright, trade secret or United States patent issued as of the date hereof, provided Manufacturer is promptly notified in writing by Customer and is given full and complete authority, information, and assistance (at Customer’s expense) for defense of same. Manufacturer shall pay damages and costs therein finally awarded against Customer but shall not be responsible for any compromise or settlement made without its written consent. In providing such defense, or in the event that such Product(s) is/are held to infringe, or the use of such Product(s) is/are enjoined, Manufacturer shall have the right in its sole discretion to obtain the right to continue using such Product(s), modify such Product(s) to become noninfringing, or require the return of such Product(s) and refund to Customer the purchase price paid by Customer to Manufacturer for such Product(s). Manufacturer’s indemnity does not extend to claims of infringement arising from Manufacturer’s compliance with Customer’s design, specifications or instructions or the modification of the Product(s) by parties other than Manufacturer or arising from the use of the Product(s) in combination with other Product(s) or in connection with a manufacturing or other process not supplied by Manufacturer. THE FOREGOING REMEDY IS EXCLUSIVE AND CONSTITUTES MANUFACTURER’S SOLE OBLIGATION FOR ANY CLAIMS OF INTELLECTUAL PROPERTY INFRINGEMENT. ### 11. LIMITATION OF LIABILITY. IN NO EVENT SHALL MANUFACTURER BE LIABLE TO CUSTOMER OR ANY THIRD PARTY FOR COSTS OF PROCUREMENT OF SUBSTITUTE GOODS, OR FOR ANY LOSS OF PROFITS OR LOSS OF USE, INCLUDING LOSS OR DAMAGE TO ANY NETWORKS, SYSTEMS, DATA OR FILES, COMPUTER FAILURE OR MALFUNCTION, OR FOR ANY INCIDENTAL, CONSEQUENTIAL, SPECIAL, PUNITIVE, EXEMPLARY, INDIRECT OR OTHER DAMAGES HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY, ARISING OUT OF THIS AGREEMENT, WHETHER OR NOT MANUFACTURER HAS BEEN ADVISED OF THE POSSIBILITY OF SUCH LOSS OR DAMAGE. THIS EXCLUSION ALSO INCLUDES ANY LIABILITY THAT MAY ARISE OUT OF THIRD-PARTY CLAIMS AGAINST CUSTOMER EXCEPT AS SET FORTH IN SECTION 9(b), MANUFACTURER ASSUMES NO OBLIGATIONS OR LIABILITY OF ANY KIND WITH RESPECT TO INFRINGEMENTS OR ALLEGED INFRINGEMENTS OF UNITED STATES OR FOREIGN PATENTS, COPYRIGHTS, TRADEMARKS, OR OTHER PROPRIETARY RIGHTS ARISING OUT OF CUSTOMER’S PURCHASE, USE, OR POSSESSION OF MANUFACTURER’S PRODUCT(S) AND CUSTOMER ASSUMES ALL SUCH RISK IN NO EVENT SHALL MANUFACTURER’S LIABILITY ARISING OUT OF THIS AGREEMENT EXCEED THE PURCHASE PRICE OF THE PRODUCT(S) PAID BY CUSTOMER TO MANUFACTURER AND SUBJECT TO THIS AGREEMENT. THE ESSENTIAL PURPOSE OF THIS PROVISION IS TO LIMIT THE POTENTIAL LIABILITY OF MANUFACTURER ARISING OUT OF THIS AGREEMENT AND/OR THE SALE OF PRODUCT(S) TO CUSTOMER, AND THE PARTIES EXPRESSLY AGREE WITH THE RESULTING ALLOCATION OF RISK. ### 12. PROPRIETARY RIGHTS, INTELLECTUAL PROPERTY AND TRADEMARKS. #### (a) Proprietary Rights. Customer acknowledges that the Product(s) sold by Manufacturer hereunder contain and embody trade secrets belonging to Manufacturer and Customer shall not reverse engineer any Product(s) purchased hereunder. In addition to the foregoing, Manufacturer owns all rights, title, and interest in and to all other intellectual property rights, including patent and copyrights, embodied by, or reflected in the Product(s). A license solely for the use of the software contained in the Product(s) is granted hereunder and Manufacturer retains for itself all proprietary rights in and to all designs, engineering details, and other data pertaining to the Product(s). #### (b) Intellectual Property. Manufacturer and Customer agree that Manufacturer shall own all right, title and interest in and to all work performed in conjunction with the Product(s) hereunder, including without limitation, ideas, discoveries, inventions, design concepts, processes, systems, computer programs, works of authorship, improvements, derivative works, and all other documentation developed for or specifically relating to the Product(s). Manufacturer hereby grants to Customer a perpetual, fully paid up, non-exclusive, non-transferable, non-sublicensable license to use the Product(s) solely for Customer’s internal business purposes. “Design Data” (including but not limited to specifications, drawings, estimates, quotations, illustrations, blueprints, bulletins, maintenance manuals, literature and other digital, electronic, or printed materials, papers, and documents) shall remain Manufacturer’s property. Manufacturer reserves all proprietary and authorship rights in the Design Data, which may not be copied, reproduced, transmitted or communicated to any third party without Manufacturer’s consent, except to Customer’s employees who are required to use Design Data as part of their duties. Manufacturer may make discretionary changes in the Design Data and may modify the Product(s) as long as such changes and/or modifications do not result in material changes in the Product(s) specifications stated in the Agreement between Customer and Manufacturer, and do not change the purchase price. #### (c) At all times hereafter, Customer agrees not to copy nor permit anyone else to copy the Product(s) or other intellectual parts thereof without written approval of Manufacturer and will not knowingly, directly, or indirectly, violate or infringe on or contest the validity of any patent, or other intellectual property or license rights of Manufacturer pertaining to any of said Product(s) or their mode of operation or any of the parts thereof. Manufacturer’s name, trademark, trade names, patent numbers, and “patent pending” designations shall not be defaced or removed from the Product(s), nor shall Customer allow such matters to be defaced or removed. #### (d) Manufacturer and Customer agree that Customer shall own all right, title and interest in and to any pre-existing works of the Customer. If any Pre-Existing Works are incorporated into or are used in conjunction with the Product(s) under this Agreement, then during the Term, Customer hereby grants to Manufacturer a fully paid up, nonexclusive, non-transferable, non-sublicensable license to use the Pre-Existing Works for incorporation into the Product(s). #### (e) Non-infringement. Customer acknowledges and agrees that Customer has the rights title and/or permissions for Intellitech to lawfully design, copy and/or modify product design data inputs, or samples, provided to Intellitech including the due diligence of potential patent, copyright, or other proprietary information infringement. Further, Customer warrants and represents that any product design data inputs and/or samples furnished to Intellitech by the Customer for use in connection with Manufacturer’s work does not infringe, misappropriate, or otherwise violate any third-party’s intellectual property rights. The Customer assumes full liability for any infringement claims of proprietary data related to any component part or design data provided to Intellitech by Customer. ### 13. IMPORT AND EXPORT REQUIREMENTS. Customer shall, at its own expense, pay all import and export licenses and permits, pay all value added and other VATs, customs charges, and duty fees, and take all other actions required to accomplish the export and import of the Product(s) purchased by Customer. Customer understands that Manufacturer may be subject to regulation by agencies of the U.S. government, including the U.S. Department of Commerce, which prohibits export or diversion of certain technical Product(s) to certain countries. Customer warrants that it will comply in all respects with the export and re-export restrictions set forth in the export license for every Product(s) shipped to Customer. ### 14. U.S. GOVERNMENT CONTRACTS. If the Product(s) to be sold hereunder are to be used in the performance of a U.S. Government contract or sub-contract and a U.S. Government contract number appears on Customer’s purchase order, those clauses of the applicable U.S. Government procurement regulation, which are mandated by Federal Statute to be included in U.S. Government subcontracts, shall be incorporated herein by reference. ### 15. CONFIDENTIALITY. Customer acknowledges that all technical or business and other documentation, information and materials delivered to or learned by Customer hereunder shall be considered Manufacturer’s confidential information (the “Confidential Information”). Customer hereby agrees: (i) to hold and maintain in strict confidence all Confidential Information of Manufacturer; and (ii) not to use any Confidential Information of Manufacturer except as permitted hereunder. Customer will use at least the same degree of care to protect the Manufacturer’s Confidential Information as it uses to protect its own confidential information of like importance, and in no event shall such degree of care be less than reasonable care. Customer agrees that it will only provide Confidential Information to those employees who have a need to know for the purposes hereunder. Customer agrees that it shall not disclose the Manufacturer Confidential Information to any third party, including third party contractors, without written authorization from Manufacturer. ### 16. MANUFACTURER’S REMEDIES FOR BREACH. (a) Customer recognizes and acknowledges that if it breaches the provisions of Section 16, damages owed to Manufacturer would be difficult, if not impossible, to ascertain. Because of the immediate and irreparable damage and loss that may be caused to Manufacturer for which it would have no adequate remedy, Customer agrees that Manufacturer, in addition to and without limiting any other remedy or right it may have, shall be entitled to seek, and receive an injunction or other equitable relief in any court of competent jurisdiction, enjoining any such breach. Customer hereby waives any and all defenses it may have on the grounds of lack of jurisdiction or competence of a court to grant such an injunction or other equitable relief. The existence of this right shall not preclude the applicability or exercise of any other rights and remedies at law or in equity which Manufacturer may have. Customer agrees that Manufacturer may obtain and shall be entitled to obtain any injunction under this Agreement without the posting of a bond. (b) In addition to any remedies set forth in this Agreement, Manufacturer shall be entitled to any and all remedies otherwise available to it under applicable law and remedies available to Manufacturer shall be considered cumulative. In the event Customer refuses or fails, for any reason, to accept any Product(s) manufactured by Manufacturer for Customer, Customer shall pay Manufacturer for all costs, including materials consumed and labor expended, to manufacture such Product(s), and Customer shall also reimburse Manufacturer for any special, incidental, or consequential damages incurred by Manufacturer because of Customer’s failure or refusal to accept delivery of such Product(s). Notwithstanding any other provision in this Agreement or in any other written document, if payment in full is not made by Customer for the Product(s) sold by Manufacturer to Customer, then Manufacturer may repossess such Product(s) by any lawful means in the event of a breach of default by Customer in any of its obligations hereunder. ### 17. FORCE MAJEURE. Manufacturer shall not be liable for damages, including liquidated damages, if any, for delays in delivery or failure to perform due to causes beyond the control and without the fault or negligence of Manufacturer. Such causes include but are not limited to, acts of God, acts of the public enemy, acts of the federal or any State or local government, fires floods, epidemics, quarantine restrictions, strikes, disturbances or embargoes. ### 18. DISPUTE RESOLUTION. (a) Parties agree to explore an amicable resolution of any dispute arising from this Agreement before either party pursues litigation. As such, the Parties agree to participate in no less than one non-binding mediation session before a neutral third- party mediator before instituting any litigation related to performance of this Contract. The Parties acknowledge their shared preference that any necessary mediation session be conducted by a retired Florida Judge or other qualified attorney mutually acceptable to the Parties. The Parties agree that the costs of the third-party mediation shall be equally shared, except that each party shall individually bear all attorneys’ fee, costs, and disbursements arising from the actions of its own counsel in conjunction with any mediation. (b) If any action at law or equity is necessary to enforce or interpret the terms of this Contract, the prevailing party shall be entitled to recover its costs and reasonable attorneys’ fees. ### 19. APPLICABLE LAW, JURY TRIAL WAIVER, JURISDICTION, AND LIMITATION ON ACTIONS. This Agreement shall be governed and construed in all respects under the laws of the State of Florida, without regard to principles of conflicts of laws. Each party hereby submits to the exclusive jurisdiction and venue of the state and federal courts sitting in the State of Florida for resolution of any dispute relating to this Agreement. The United Nations Convention on the International Sale of Goods shall not apply to this Agreement or to any of the transactions contemplated hereby. THE PARTIES HEREBY IRREVOCABLY AND KNOWINGLY WAIVE TO THE FULLEST EXTENT PERMITTED BY LAW ANY RIGHT TO A TRIAL BY JURY IN ANY ACTION OR PROCEEDING ARISING OUT OF THIS AGREEMENT. The parties agree that any such action or proceeding shall be tried before a court and not a jury. The parties hereby irrevocably and unconditionally submit to the jurisdiction of the Courts of the State of Florida and of the United States of America for the District of Florida and agree that any legal action or proceeding relating to this Agreement may be brought in such courts. In the event the parties’ waiver of a trial by jury is deemed invalid, the parties hereby agree that any action or claim arising out of any dispute in connection with this Agreement, any rights, remedies, obligations, or duties hereunder, or the performance or enforcement hereof or thereof shall be deter- mined by judicial reference. Customer shall not bring any action relating to any dispute Customer may have after one (1) year of the accrual of such dispute. ### 20. ATTORNEYS’ FEES. In the event litigation shall be instituted to enforce any provision of this Agreement, the prevailing party in such litigation shall be entitled to recover reasonable attorneys’ fees and expenses incurred in such litigation, including on appeal, in addition to any other recovery to which such party may be legally entitled. ### 21. INSTALLATION AND COMMISSIONING. Installation and commissioning services are available by separately executed agreement. ### 22. SUBSTITUTIONS AND MODIFICATIONS. Manufacturer reserves the right to (i) make substitutions and modifications in the specifications of Product(s) sold by Manufacturer, provided that such substitutions or modifications do not materially affect overall Product(s) performance, and (ii) discontinue or otherwise end-of-life any Product(s) sold hereunder. ### 23. NO PARTNERSHIP OR AGENCY. Nothing in this Agreement shall (i) be deemed a partnership in law between the Parties, (ii) constitute either party an agent of the other for any purpose or (iii) entitle either party to commit or bind the other (or any member of its respective group) in any manner. ### 24. NOTICES. Any notice contemplated by or made pursuant to this Agreement shall be in writing and shall be deemed delivered on the date of delivery if delivered personally, or three (3) days after mailing if placed in the U.S. mail, postage prepaid, registered, or certified mail, return receipt requested, addressed to Customer or Manufacturer (as the case may be) at the designated address, or such other address as shall be designated by at least ten (10) days prior written notice. A notice given by any means other than as specified herein will be deemed duly given when received by the addressee. ### 25. SEVERABILITY. If any provision of this Agreement or the application thereof to any party or circumstance is held to be invalid, illegal, or unenforceable in any respect, that provision to that extent shall be severed from this Agreement (but, to the extent permitted by law, not otherwise), and shall not affect the remainder hereof, and the Parties agree to substitute for such provision a valid provision which most closely approximates the intent and economic effect of such severed provision. ### 26. ASSIGNMENT. (a) Customer may not assign its rights or obligations hereunder without the prior written consent of Manufacturer, which may not be unreasonably withheld. This Agreement shall be binding upon and inure to the benefit of the Parties hereto and their respective heirs, personal representatives, successors and assigns. (b) Manufacturer may subcontract or assign any or all of its obligations under this Agreement in its sole discretion. It is understood, however, that Manufacturer remains responsible for compliance with its obligations under this Agreement including conformance of the Product(s) to the requirements set forth herein. ### 27. ERRORS AND VALIDITY OF AGREEMENT. Stenographic and clerical errors in sales made under this Agreement are subject to correction. In the event any provision of this Agreement is held to be invalid or unenforceable, then such provision shall be deemed automatically adjusted to the minimum extent necessary to conform to the requirements for validity as declared at such time and, as so adjusted, shall be deemed a provision of this Agreement as though originally included herein. In the event that the provision invalidated is of such a nature that it cannot be so adjusted, the provision shall be deemed deleted from this Agreement as though such provision had never been included herein. In either case, the remaining provisions of this Agreement will remain in full force and effect. ### 28. WAIVER AND MODIFICATION. No delay or failure by either party to exercise or enforce at any time any right or provision hereof will be considered a waiver thereof of such party’s rights thereafter to exercise or enforce each and every right and provision hereof. No single waiver will constitute a continuing or subsequent waiver. No waiver, modification or amendment of any provision hereof will be effective unless it is in a signed writing by the Parties. No representative, agent, salesperson, or service engineer is authorized by Manufacturer to give any guaranty, warranty or to make any representation contrary to these Terms and Conditions. Only a duly authorized officer of Manufacturer can modify or alter these Terms and Conditions and such modification can only be in a writing signed by the Parties. ### 29. SURVIVAL. The Parties acknowledge and agree that any provision that by its nature survives shall survive cancellation or termination of this Agreement. ### 30. ENTIRE AGREEMENT. The terms and conditions set forth herein constitute the entire Agreement between Customer and Manufacturer and supersede any other agreements or offers, including any purchase order of Customer, prior or contemporaneous oral or written understandings, or communications relating to the subject matter hereof. Notwithstanding the foregoing, in the event Customer and Manufacturer have a written Supply Agreement, the terms of the Supply Agreement shall govern. --- ### [Single-Use Assemblies](https://intellitech-inc.com/single-use-assemblies/) **Published:** December 1, 2023 **Author:** craig **Content:** # Single-Use Assemblies ## ## Custom Single-Use Assemblies for Bioprocessing and Biopharmaceutical Manufacturing Our **single-use assemblies**, within custom single use systems, have various applications in biopharmaceutical development and production such as cell culturing, sampling, mixing, filtration, and fill/finish. According to a survey by BioPlan Associates, over 85% of biopharmaceutical manufacturers use single-use systems in their production process. This effectively eliminates the high energy cost of clean-in-place/sterilization-in-place (CIP/SIP) protocols, resulting in improvements in sustainability. [Contact us today](https://intellitech-inc.com/request-a-quote/) for a custom single-use system for your bioprocessing and biomanufacturing needs. ### Single-Use Bag Assemblies **Bioprocessing bag assemblies** play a crucial role in the development of biologic and pharmaceutical drug products. In bioprocessing, these single-use bags are often used for applications such as product mixing, collection, storage, transfer, or transport. Bag materials are made to hold biologics, media, and other materials as a part of bioprocess container systems. Intellitech can offer these bioprocess bags in 2D and 3D configurations and customize tubing and fittings to meet the requirements of a specific application. ![EGMO 2D single use bag assemblies  ](https://intellitech-inc.com/wp-content/uploads/2023/02/Bag-2-683x1024.png "Bag 2 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ![tubing sets](https://intellitech-inc.com/wp-content/uploads/2021/04/custom-samples-new2.png "custom-samples-new2 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Single-Use Bottle Assemblies Similar to single-use bags, sterile bottles are also important in biologic production. These **bioprocess containers** are made for use in product mixing, sampling, storage, transport, bioreactors, and more. These bottles are also made to handle biopharmaceuticals as well as other bioprocess materials. Intellitech collaborates with its customers to determine the appropriate bottle size, material, and closure configuration to meet the requirements of their application. ### Request a Quote ##### Innovative solutions that are custom configured to meet your needs. Contact us today to build a custom single-use system that meets your requirements. [ Request a Quote ](/request-a-quote/) ### Single-Use Filtration Assemblies **Single-use filter assemblies** play a critical role in bioprocessing applications. They ensure that biological process fluids are sterile and that consistent pressure conditions remain in the processing tank or fluid path. They are commonly used in various single-use assemblies for upstream and downstream processing. Intellitech can supply these filters and incorporate them into designs according to our customer’s application and requirements. ### Single-Use Tubing and Manifold Assemblies Choosing the right **single-use tubing assemblies**, fittings, and connectors are critical for fluid management in bioprocessing applications. Sizing and materials must be carefully chosen to ensure proper fluid flow, sterility, and reduce the risk of leaks. Intellitech can offer many different fittings and connectors to meet the requirements of our customers. These parts also feature animal-derivative-free materials and meet USP Class VI requirements, both of which are important requirements for biopharmaceutical manufacturing. For more complex applications, we can provide bioprocess manifolds that simplify your fluid path and reduce the number of connections. ### Single-Use Filling Assemblies Our **single-use filling assemblies** are vital in bio/pharma development, comprising of a needle, hub, and sometimes a guard/sheath. Filling needle assemblies by Intellitech expertly facilitate precise liquid transfer while maintaining sterility. Intellitech can offer filling needles that come in many different configurations. For filling operations that are large or small, we work with our customers to meet their process requirements. ### Mixing & Sampling “Experience seamless precision and unparalleled control in your bio/pharma operations with our cutting-edge needle assemblies and tubing connectors. **Mixing Excellence:** Our needle assemblies are engineered to deliver precision in transferring vital components during pharmaceutical formulation and bioprocessing. Ensure consistent dosages and homogeneous blends with our reliable assemblies, optimizing your mixing processes for superior product quality. **Seamless Sampling:** Elevate your quality control with our needle assemblies designed for precise and representative sample extraction. Coupled with our high-quality tubing connectors, seamlessly direct samples between instruments and testing points. Ensure accuracy and maintain the integrity of your analyses, adhering to the highest standards in sampling protocols. From ensuring uniformity in mixtures to maintaining the fidelity of your sampling procedures, our needle assemblies and tubing connectors are the backbone of reliability and precision in bio/pharma operations. Partner with us to elevate your processes and guarantee the quality and consistency of your pharmaceutical products.” ### Request a Quote ##### Innovative solutions that are custom configured to meet your needs. Contact us today to build a custom liquid filling machine with tighter fill tolerances to suit you. [ Request a quote ](/request-a-quote/) #### Interested in learning more? Please provide your contact information. Name(Required) First Last Email(Required) Your Business Name(Required) Your Business Website Message(Required) CAPTCHA Submit ## Intellitech Products Many of our customers are involved in biologic drug/therapy/vaccine R&D and transitioning to GMP production and we, at Intellitech, believe we can best support those efforts by continuing to focus on manufacturing and improving the i-FILL family of precision liquid dispensing pump technology and single-use systems. #### Single Use Assemblies ### Single Use Assemblies Intellitech has unique experience in the design, development and manufacture of many assemblies used in BIO/PHARMA development and production. [Read More](https://intellitech-inc.com/single-use-assemblies/) #### Fluid/Cell Transfer Pump ### Fluid/Cell Transfer Pump The i-Fill® pump is proven effective to transfer live cells with little to no effect on the cells after varying tested periods of time. [Read More](https://intellitech-inc.com/fluid-cell-transfer-pump/) #### Precision Filling Pump ### Precision Filling Pump The i-Fill® delivers unmatched, repeatable dispense accuracy over thousands of dispenses for volumes of 100mcL to 100mL. [Read More](https://intellitech-inc.com/precision-filling-pump/) --- ### [Testing & Validation Service](https://intellitech-inc.com/testing-validation/) **Published:** November 19, 2024 **Author:** craig **Content:** # Testing & Validation Service ## Tested and Validated Single-Use Systems. Intellitech’s Testing and Validation Services ensures the highest quality and reliability of single-use systems. We achieve this through testing and validating against industry standards and regulatory requirements. ![](https://intellitech-inc.com/wp-content/uploads/2024/11/icon-outlined-Testing-Validation-Services.webp "icon-outlined-Testing-Validation-Services - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Product Testing Services Intellitech can support customers in providing pressure testing of single-use systems, which is used to detect leaks and ensure the integrity of the assembly. By employing pressure decay testing, we can help customers prevent contamination, product loss, and costly production delays due to faulty fluid management components. ### Validation Services Intellitech collaborates with an accredited 3rd party testing lab to perform validation studies on processes to define critical quality attributes and acceptance criteria for single-use systems. - Package Integrity Validation - ASTM F2097 Bubble Emission Testing - ASTM F88 Seal Strength Testing - ASTM F1929 Dye Penetration Testing - ASTM F1980 Accelerated Aging and Real Time Aging for Shelf-life Validation - ANSI/AAMI/ISO 11737-1:2018 Bioburden Testing - ANSI/AAMI/ISO 11137-2:2013 Sterilization Dose Audit ### Ready to Get Started? #### Contact us today to learn more about how we can streamline your single-use process needs. [ Contact Us ](/contact-us/) ## Explore Intellitech's Services #### Intellitech Covers The Spectrum To Support Customers From R&D To GMP. [![](https://intellitech-inc.com/wp-content/uploads/2024/11/design-engineering-icon.webp "design-engineering-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/design-engineering/)### [Design & Engineering Services](/design-engineering/) [ Learn More ](/design-engineering/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/prototyping-fabrication-icon.webp "prototyping-fabrication-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/prototyping-fabrication/)### [Prototyping & Fabrication Services](/prototyping-fabrication/) [ Learn More ](/prototyping-fabrication/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/assembly-packaging-icon.webp "assembly-packaging-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/cleanroom-assembly-packaging/)### [Cleanroom Assembly & Packaging Services](/cleanroom-assembly-packaging/) [ Learn More ](/cleanroom-assembly-packaging/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/testing-validation-icon.webp "testing-validation-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/testing-validation/)### [Testing & Validation Services](/testing-validation/) [ Learn More ](/testing-validation/) --- ### [Prototyping & Fabrication Service](https://intellitech-inc.com/prototyping-fabrication/) **Published:** November 19, 2024 **Author:** craig **Content:** # Prototyping & Fabrication Service ## High-quality Single-Use System prototypes for Biopharma. Intellitech’s Prototyping & Fabrication Service delivers high-quality prototypes with streamlined development, comprehensive documentation, and seamless transition to manufacturing. ![](https://intellitech-inc.com/wp-content/uploads/2024/11/icon-outlined-Prototyping-Fabrication-Services.webp "icon-outlined-Prototyping-Fabrication-Services - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Streamlined Development Intellitech is capable of delivering advanced prototypes of single-use systems with development lab bench-built first articles, CNC-machining, and/or 3D printing. Customers can leverage our prototyping services to streamline the development process of these designs. Manufacturing documentation is also captured in parallel with prototyping, ensuring a smooth transition into GMP manufacturing. Our customers can then take advantage of our assembly and packaging services that we perform in our ISO7-certified cleanroom environments. ### Headline Coming Soon Lorem ipsum dolor sit amet, consectetur adipiscing elit. Maecenas in quam quis ligula volutpat fringilla et fringilla libero. Phasellus ut risus quam. Sed ullamcorper ante nec lorem tempor, vel tincidunt magna mollis. Maecenas iaculis sem et lorem varius, vestibulum efficitur sapien maximus. Duis gravida lacus et lacus ultrices sodales. Sed ac felis scelerisque, blandit tellus et, molestie nisl. Nulla feugiat rhoncus ligula. Nullam scelerisque metus a neque ultricies dignissim. Duis malesuada arcu vel commodo. ### Cleanroom Assembly & Packaging Service #### Intellitech manufactures and packages single-use systems in an ISO7 Cleanroom to ensure clean, high-quality products that meet your specifications. [ Read More ](/cleanroom-assembly-packaging/) ## Explore Intellitech's Services #### Intellitech Covers The Spectrum To Support Customers From R&D To GMP. [![](https://intellitech-inc.com/wp-content/uploads/2024/11/design-engineering-icon.webp "design-engineering-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/design-engineering/)### [Design & Engineering Services](/design-engineering/) [ Learn More ](/design-engineering/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/prototyping-fabrication-icon.webp "prototyping-fabrication-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/prototyping-fabrication/)### [Prototyping & Fabrication Services](/prototyping-fabrication/) [ Learn More ](/prototyping-fabrication/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/assembly-packaging-icon.webp "assembly-packaging-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/cleanroom-assembly-packaging/)### [Cleanroom Assembly & Packaging Services](/cleanroom-assembly-packaging/) [ Learn More ](/cleanroom-assembly-packaging/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/testing-validation-icon.webp "testing-validation-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/testing-validation/)### [Testing & Validation Services](/testing-validation/) [ Learn More ](/testing-validation/) --- ### [Products](https://intellitech-inc.com/products/) **Published:** December 24, 2024 **Author:** craig **Content:** # Products ## Custom Single-Use and Pump Solutions. ### Tailor-made for BIO/PHARMA. At Intellitech, we specialize in designing and manufacturing custom single-use systems and precision dispensing pumps for the biopharmaceutical industry. All of Intellitech’s products can be tailored to meet your unique application and requirements. ![.](https://intellitech-inc.com/wp-content/uploads/2025/06/intellitech-logo-stacked-2025.png "intellitech-logo-stacked-2025 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ![Product-SingleUse](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/Product-SingleUse-qyzm0vfcg05nxj33dxq45hs0pwn8hubx2nfp9jgtfk.webp "Product-SingleUse") ### Single-Use Systems Single-Use Assemblies have various applications in biopharmaceutical development production such as cell culturing, sampling, mixing, filtration, and fill/finish. [ Learn More ](/single-use-systems/) ![live cell transfer pump Cleanroom Assembly i-FILL i-FILL Micro](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/iFIll-Micro-ql9j0tgqa3uiz74dudsv8k2cppu5gngl98pfhw6qkg.png "iFIll-Micro") ### i-FILL Micro The i-FILL® Micro is a precision pump designed for accurate, repeatable small- volume filling. This is ideal for handling delicate product and fill volumes up to 15mL. [ Learn More ](/i-fill-micro/) ![Product-i-fill-image](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/Product-i-fill-image-qz2v34xtrl60z9mr1kq581egl52n0oo1tblweexog0.webp "Product-i-fill-image") ### i-FILL The i-FILL® is a precision pump designed for accurate and repeatable large-volume filling. This is ideal for efficient product transfer and fill volumes up to 100mL. [ Learn More ](/i-fill/) ### We welcome the opportunity to work with you ##### We support companies spanning the realm of R&D to GMP with a range of products and services. Call **1-727-914-7000** or [**contact us**](/contact-us/) to share your project, goals, and challenges. [ Contact Us ](/contact-us/) --- ### [Privacy Policy](https://intellitech-inc.com/privacy-policy/) **Published:** May 13, 2021 **Author:** craig **Content:** # Privacy Policy This Privacy Policy describes Our policies and procedures on the collection, use and disclosure of Your information when You use the Service and tells You about Your privacy rights and how the law protects You. We use Your Personal data to provide and improve the Service. By using the Service, You agree to the collection and use of information in accordance with this Privacy Policy. This Privacy Policy has been created with the help of the Privacy Policy Generator. ## Interpretation and Definitions #### Interpretation The words of which the initial letter is capitalized have meanings defined under the following conditions. The following definitions shall have the same meaning regardless of whether they appear in singular or in plural. #### Definitions For the purposes of this Privacy Policy: - **Account** means a unique account created for You to access our Service or parts of our Service. - **Company** (referred to as either “the Company”, “We”, “Us” or “Our” in this Agreement) refers to Intellitech, Inc., 11801 28th St. N, #5, St. Petersburg, FL 33716. - **Cookies** are small files that are placed on Your computer, mobile device or any other device by a website, containing the details of Your browsing history on that website among its many uses. - **Country** refers to: Florida, United States - **Device** means any device that can access the Service such as a computer, a cellphone or a digital tablet. - **Personal Data** is any information that relates to an identified or identifiable individual. - **Service** refers to the Website. - **Service Provider** means any natural or legal person who processes the data on behalf of the Company. It refers to third-party companies or individuals employed by the Company to facilitate the Service, to provide the Service on behalf of the Company, to perform services related to the Service or to assist the Company in analyzing how the Service is used. - **Usage Data** refers to data collected automatically, either generated by the use of the Service or from the Service infrastructure itself (for example, the duration of a page visit). - **Website** refers to Intellitech Precision Liquid Filling, accessible from www.intellitech-inc.com - **You** means the individual accessing or using the Service, or the company, or other legal entity on behalf of which such individual is accessing or using the Service, as applicable. ## Collecting and Using Your Personal Data ### Types Of Data Collected #### Personal Data While using Our Service, We may ask You to provide Us with certain personally identifiable information that can be used to contact or identify You. Personally identifiable information may include, but is not limited to: - Email address - First name and last name - Phone number - Usage Data #### Usage Data Usage Data is collected automatically when using the Service. Usage Data may include information such as Your Device’s Internet Protocol address (e.g. IP address), browser type, browser version, the pages of our Service that You visit, the time and date of Your visit, the time spent on those pages, unique device identifiers and other diagnostic data. When You access the Service by or through a mobile device, We may collect certain information automatically, including, but not limited to, the type of mobile device You use, Your mobile device unique ID, the IP address of Your mobile device, Your mobile operating system, the type of mobile Internet browser You use, unique device identifiers and other diagnostic data. We may also collect information that Your browser sends whenever You visit our Service or when You access the Service by or through a mobile device. #### Tracking Technologies And Cookies We use Cookies and similar tracking technologies to track the activity on Our Service and store certain information. Tracking technologies used are beacons, tags, and scripts to collect and track information and to improve and analyze Our Service. The technologies We use may include: - **Cookies or Browser Cookies.** A cookie is a small file placed on Your Device. You can instruct Your browser to refuse all Cookies or to indicate when a Cookie is being sent. However, if You do not accept Cookies, You may not be able to use some parts of our Service. Unless you have adjusted Your browser setting so that it will refuse Cookies, our Service may use Cookies. - **Flash Cookies.** Certain features of our Service may use local stored objects (or Flash Cookies) to collect and store information about Your preferences or Your activity on our Service. Flash Cookies are not managed by the same browser settings as those used for Browser Cookies. For more information on how You can delete Flash Cookies, please read “Where can I change the settings for disabling, or deleting local shared objects?” available at https://helpx.adobe.com/flash-player/kb/disable-local-shared-objects-flash.html#main\_Where\_can\_I\_change\_the\_settings\_for\_disabling\_\_or\_deleting\_local\_shared\_objects\_ - **Web Beacons.** Certain sections of our Service and our emails may contain small electronic files known as web beacons (also referred to as clear gifs, pixel tags, and single-pixel gifs) that permit the Company, for example, to count users who have visited those pages or opened an email and for other related website statistics (for example, recording the popularity of a certain section and verifying system and server integrity). Cookies can be “Persistent” or “Session” Cookies. Persistent Cookies remain on Your personal computer or mobile device when You go offline, while Session Cookies are deleted as soon as You close Your web browser. Learn more about cookies: Cookies: What Do They Do?. We use both Session and Persistent Cookies for the purposes set out below: - **Necessary / Essential Cookies**Type: Session Cookies Administered by: Us Purpose: These Cookies are essential to provide You with services available through the Website and to enable You to use some of its features. They help to authenticate users and prevent fraudulent use of user accounts. Without these Cookies, the services that You have asked for cannot be provided, and We only use these Cookies to provide You with those services. - **Cookies Policy / Notice Acceptance Cookies**Type: Persistent Cookies Administered by: Us Purpose: These Cookies identify if users have accepted the use of cookies on the Website. - **Functionality Cookies**Type: Persistent Cookies Administered by: Us Purpose: These Cookies allow us to remember choices You make when You use the Website, such as remembering your login details or language preference. The purpose of these Cookies is to provide You with a more personal experience and to avoid You having to re-enter your preferences every time You use the Website. For more information about the cookies we use and your choices regarding cookies, please visit our Cookies Policy or the Cookies section of our Privacy Policy. ### Use Of Your Personal Data The Company may use Personal Data for the following purposes: - **To provide and maintain our Service**, including to monitor the usage of our Service. - **To manage Your Account:** to manage Your registration as a user of the Service. The Personal Data You provide can give You access to different functionalities of the Service that are available to You as a registered user. - **For the performance of a contract:** the development, compliance and undertaking of the purchase contract for the products, items or services You have purchased or of any other contract with Us through the Service. - **To contact You:** To contact You by email, telephone calls, SMS, or other equivalent forms of electronic communication, such as a mobile application’s push notifications regarding updates or informative communications related to the functionalities, products or contracted services, including the security updates, when necessary or reasonable for their implementation. - **To provide You** with news, special offers and general information about other goods, services and events which we offer that are similar to those that you have already purchased or enquired about unless You have opted not to receive such information. - **To manage Your requests:** To attend and manage Your requests to Us. - **For business transfers:** We may use Your information to evaluate or conduct a merger, divestiture, restructuring, reorganization, dissolution, or other sale or transfer of some or all of Our assets, whether as a going concern or as part of bankruptcy, liquidation, or similar proceeding, in which Personal Data held by Us about our Service users is among the assets transferred. - **For other purposes**: We may use Your information for other purposes, such as data analysis, identifying usage trends, determining the effectiveness of our promotional campaigns and to evaluate and improve our Service, products, services, marketing and your experience. We may share Your personal information in the following situations: - **With Service Providers:** We may share Your personal information with Service Providers to monitor and analyze the use of our Service, to contact You. - **For business transfers:** We may share or transfer Your personal information in connection with, or during negotiations of, any merger, sale of Company assets, financing, or acquisition of all or a portion of Our business to another company. - **With Affiliates:** We may share Your information with Our affiliates, in which case we will require those affiliates to honor this Privacy Policy. Affiliates include Our parent company and any other subsidiaries, joint venture partners or other companies that We control or that are under common control with Us. - **With business partners:** We may share Your information with Our business partners to offer You certain products, services or promotions. - **With other users:** when You share personal information or otherwise interact in the public areas with other users, such information may be viewed by all users and may be publicly distributed outside. - **With Your consent**: We may disclose Your personal information for any other purpose with Your consent. ### Retention Of Your Personal Data The Company will retain Your Personal Data only for as long as is necessary for the purposes set out in this Privacy Policy. We will retain and use Your Personal Data to the extent necessary to comply with our legal obligations (for example, if we are required to retain your data to comply with applicable laws), resolve disputes, and enforce our legal agreements and policies. The Company will also retain Usage Data for internal analysis purposes. Usage Data is generally retained for a shorter period of time, except when this data is used to strengthen the security or to improve the functionality of Our Service, or We are legally obligated to retain this data for longer time periods. ### Transfer Of Your Personal Data Your information, including Personal Data, is processed at the Company’s operating offices and in any other places where the parties involved in the processing are located. It means that this information may be transferred to — and maintained on — computers located outside of Your state, province, country or other governmental jurisdiction where the data protection laws may differ than those from Your jurisdiction. Your consent to this Privacy Policy followed by Your submission of such information represents Your agreement to that transfer. The Company will take all steps reasonably necessary to ensure that Your data is treated securely and in accordance with this Privacy Policy and no transfer of Your Personal Data will take place to an organization or a country unless there are adequate controls in place including the security of Your data and other personal information. ### Disclosure Of Your Personal Data #### Business Transactions If the Company is involved in a merger, acquisition or asset sale, Your Personal Data may be transferred. We will provide notice before Your Personal Data is transferred and becomes subject to a different Privacy Policy. #### Law Enforcement Under certain circumstances, the Company may be required to disclose Your Personal Data if required to do so by law or in response to valid requests by public authorities (e.g. a court or a government agency). #### Other Legal Requirements The Company may disclose Your Personal Data in the good faith belief that such action is necessary to: - Comply with a legal obligation - Protect and defend the rights or property of the Company - Prevent or investigate possible wrongdoing in connection with the Service - Protect the personal safety of Users of the Service or the public - Protect against legal liability ### Security Of Your Personal Data The security of Your Personal Data is important to Us, but remember that no method of transmission over the Internet, or method of electronic storage is 100% secure. While We strive to use commercially acceptable means to protect Your Personal Data, We cannot guarantee its absolute security. ## Children’s Privacy Our Service does not address anyone under the age of 13. We do not knowingly collect personally identifiable information from anyone under the age of 13. If You are a parent or guardian and You are aware that Your child has provided Us with Personal Data, please contact Us. If We become aware that We have collected Personal Data from anyone under the age of 13 without verification of parental consent, We take steps to remove that information from Our servers. If We need to rely on consent as a legal basis for processing Your information and Your country requires consent from a parent, We may require Your parent’s consent before We collect and use that information. ## Links to Other Websites Our Service may contain links to other websites that are not operated by Us. If You click on a third party link, You will be directed to that third party’s site. We strongly advise You to review the Privacy Policy of every site You visit. We have no control over and assume no responsibility for the content, privacy policies or practices of any third party sites or services. ## Changes to this Privacy Policy We may update Our Privacy Policy from time to time. You are advised to review this Privacy Policy periodically for any changes. Changes to this Privacy Policy are effective when they are posted on this page. ## Contact Us If you have any questions about this Privacy Policy, You can contact us: - [ Contact Us ](/contact-us/) - [ 727-914-7000 ](tel:727-914-7000) --- ### [Our Quality Policy](https://intellitech-inc.com/our-quality-policy/) **Published:** November 18, 2024 **Author:** craig **Content:** # Our Quality Policy ## Intellitech covers the spectrum to support customers from R&D to GMP for single-use systems. ### Our Committment Intellitech is committed to satisfying customers through the on-time delivery of products that meet requirements while continuously improving the effectiveness of our Quality Management System (QMS). Intellitech’s quality policy is broken down into four, high-level objectives to ensure we meet these commitments: - Customer Fulfillment / Product Quality - Effectiveness of Our QMS - Continuous QMS Improvements - Continuous Process Improvements Intellitech maintains an ISO9001:2015-certified QMS as well as thorough process control and documentation to adhere to GMP guidelines. Intellitech also maintains an ISO7-certified cleanroom manufacturing area, which is qualified by a third-party testing firm. See Our ISO9001:2015 Certification ### Documentation #### Intellitech creates, approves, releases, and maintains the required documentation to meet GMP requirements. As a qualified supplier to top pharmaceutical manufacturers, Intellitech creates, approves, releases, and maintains the appropriate documentation to meet Good Manufacturing Practice (GMP) requirements. This includes drawings, Bill of Materials, work instructions, data collection forms, batch records, and Certificates of Conformance. Intellitech’s document control system employs a validated electronic workflow that meets the requirements of 21 CFR 820. ### We welcome the opportunity to work with you #### We support companies spanning the realm of R&D to GMP with a range of products and services. Call **[1-727-914-7000](tel:17279147000)** or [**contact us**](https://intellitech-inc.com/contact-us/) to share your project, goals, and challenges. [ Contact Us ](/contact-us/) ### Product Quality Product quality is one of Intellitech’s top priorities. Ensuring high product quality requires control over key areas of the manufacturing process. Our experienced Quality Department performs inspections in key areas, ensuring all products that we produce are of the highest quality and that they meet the requirements of our customers. This includes inspections on: - Incoming Material - Assemblies - Packaged Products - Packaged Products After Sterilization Intellitech also identifies and qualifies suppliers of component parts. We continually monitor our suppliers to meet requirements for on-time delivery and rejected material. These are critical aspects of GMP. ### Process Control In nearly every process that Intellitech performs, we have procedures and methods of documentation in place to capture data and ensure high product quality. Examples of where process control is exerted: - Non-Conforming Outputs, Deviations, and Incidents - Manufacturing Processes, Documents, and Design Changes - Process Monitoring and Measuring Equipment Issues can always occur, despite controls. Intellitech ensures that quality issues are identified and resolved prior to shipment to the customer. If, however, a customer identifies a nonconforming product, Intellitech works closely with the customer to capture feedback, returns, and determine the best corrective action to resolve any issue. ### Trained Operators Intellitech’s Cleanroom Technicians are thoroughly trained on Intellitech’s Single-Use manufacturing processes. They are also subject to occasional competency checks, ensuring all technicians are consistently receiving up-to-date training to maintain high product quality. ### Process Control In nearly every process that Intellitech preforms, we have procedures and methods of documentation in place to capture data and ensure high product quality. Examples of where process control is exerted: - Non-Conforming Outputs, Deviations, and Incidents - Manufacturing Processes, Documents, and Design Changes - Process Monitoring and Measuring Equipment Issues can always occur, despite controls. Intellitech ensures that quality issues are identified and resolved prior to shipment to the customer. If, however, a customer identifies a nonconforming product, Intellitech works closely with the customer to capture feedback, returns, and determine the best corrective action to resolve any issue. ### Trained Operators Intellitech’s Cleanroom Operators are throughly trained on Intellitech’s Single-Use manufacturing processes. They are also subject to occasional competency checks, ensuring all operators are consistently receiving up-to-date training to maintain high product quality. --- ### [Our Services](https://intellitech-inc.com/services/) **Published:** November 18, 2024 **Author:** craig **Content:** # Our Services ## Custom Single-Use Systems, Made Simple. ### Efficient. Experienced. Qualified. Intellitech designs and manufactures custom single use systems for the biopharmaceutical industry. Can’t find a single use assembly that fits your application? We make it easy to take a design concept from a simple sketch to a GMP-compliant product. ![.](https://intellitech-inc.com/wp-content/uploads/2025/06/intellitech-logo-stacked-2025.png "intellitech-logo-stacked-2025 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ![icon-Design-Engineering-Services](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/icon-Design-Engineering-Services-qx997wqcrpavt4fac36vod3f3dggsogszm8gm5njls.webp "icon-Design-Engineering-Services") ### Design & Engineering Services Intellitech is set apart by its robust design process for custom single-use systems. Experienced in providing single-use assemblies to many biopharma companies, Intellitech has developed an efficient and thorough process for design and development. [ Learn More ](/design-engineering/) ![icon-Prototyping-Fabrication-Services](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/icon-Prototyping-Fabrication-Services-qx99kvw54d2e3bkpk74gll7ibvhw28zefugs4oevpc.webp "icon-Prototyping-Fabrication-Services") ### Prototyping & Fabrication Services Intellitech works with you to determine the best design based on your requirements. We make sure that the materials, packaging, sterilization, and product testing matches your application. We also offer prototyping and fabrication services for initial proof-of-concept and product testing. [ Learn More ](/prototyping-fabrication/) ![icon-Cleanroom-Assembly-Packaging-Services](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/icon-Cleanroom-Assembly-Packaging-Services-qx99mbl9k915tvhm6bgxwq5v02f2tlomyychiwa874.webp "icon-Cleanroom-Assembly-Packaging-Services") ### Cleanroom Assembly & Packaging Services Intellitech’s Cleanroom Assembly and Packaging Service puts our customers at ease. Our manufacturing environments and processes are highly controlled so that our single-use assembly and packaging meets strict sterility and bioburden requirements. [ Learn More ](/cleanroom-assembly-packaging/) ![icon-Testing-Validation-Services](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/icon-Testing-Validation-Services-qx99mlxhnffbdl2lhxxu65jxjb0469tooditsxuwao.webp "icon-Testing-Validation-Services") ### Testing & Validation Services Intellitech collaborates with a 3rd party testing laboratory to provide you with testing and validation services for your single use systems such as pressure decay testing, package integrity testing, bio-burden testing, dose-auditing, and more. [ Learn More ](/testing-validation/) ### We welcome the opportunity to work with you ##### We support companies spanning the realm of R&D to GMP with a range of products and services. Call **1-727-914-7000** or [**contact us**](/contact-us/) to share your project, goals, and challenges. [ Contact Us ](/contact-us/) --- ### [Meet the Team](https://intellitech-inc.com/meet-the-team/) **Published:** January 3, 2025 **Author:** craig **Content:** # Meet the Team ## Biopharmaceutical Solutions Simplified. ### Innovative. Collaborative. Reliable. At Intellitech, we specialize in crafting tailored single-use systems for the biopharmaceutical industry. Have a unique process need? Our team thrives on bringing creative designs to life, delivering GMP-compliant products with precision and care. ![](https://intellitech-inc.com/wp-content/uploads/2024/11/IntelliTech-Logo-stacked-2024.png "IntelliTech-Logo-stacked-2024 - Intellitech Inc | Innovators of Single-Use Liquid Filling") - ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-BarbaraBiller.webp) - ![]( "Barbara Biller") Barbara Biller President Lorem ipsum dolor sit amet, consectetur adipiscing elit. Nullam id eros sit amet velit gravida auctor. Suspendisse fringilla, lorem at varius congue, sapien sapien convallis eros, sit amet aliquet est quam id eros. Curabitur laoreet, purus et volutpat suscipit, felis libero hendrerit ipsum, a fermentum metus elit in urna. Sed vehicula, nisi non luctus porttitor, lectus lectus luctus elit, nec cursus enim nisi vitae nisl. Suspendisse potenti. Donec quis mi nec eros tincidunt sodales. Pellentesque interdum sapien id ante dictum, at interdum odio volutpat. Ut eu sapien nec sapien placerat ultrices. Curabitur at nunc malesuada, posuere mi et, egestas est. Aliquam erat volutpat. Nam non purus ac urna facilisis pretium sit amet id velit. Fusce malesuada mauris id libero eleifend, id aliquet mi pharetra. Suspendisse ornare, ex non maximus fringilla, justo libero facilisis lorem, quis efficitur nisl ipsum vel tortor. Nam non purus ac urna facilisis pretium sit amet id velit. - ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-AnthonyBiller.webp) - ![]( "Anthony Biller") Anthony Biller Director of New Business Development Vestibulum ante ipsum primis in faucibus orci luctus et ultrices posuere cubilia curae; Integer ut elit id lorem fermentum auctor non sit amet elit. Vivamus convallis euismod elit id vulputate. Integer id felis ac lacus dapibus ultrices. Proin id interdum tortor. Duis in justo neque. Sed vehicula tincidunt risus, non interdum lectus fermentum nec. Nullam vitae lorem a arcu eleifend tincidunt vitae eu nibh. Curabitur laoreet, purus et volutpat suscipit, felis libero hendrerit ipsum, a fermentum metus elit in urna. Phasellus lacinia, arcu non hendrerit ultricies, odio magna laoreet sem, a volutpat metus quam a felis. Nam varius fermentum nulla, eget auctor justo interdum id. Suspendisse potenti. Donec quis mi nec eros tincidunt sodales. Pellentesque interdum sapien id ante dictum, at interdum odio volutpat. Aenean in tempor enim, vitae laoreet mauris. Donec quis mi nec eros tincidunt sodales. Nullam id eros sit amet velit gravida auctor. - ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-BarbaraBiller.webp "Barbara Biller") Barbara Biller President Lorem ipsum dolor sit amet, consectetur adipiscing elit. Nullam id eros sit amet velit gravida auctor. Suspendisse fringilla, lorem at varius congue, sapien sapien convallis eros, sit amet aliquet est quam id eros. Curabitur laoreet, purus et volutpat suscipit, felis libero hendrerit ipsum, a fermentum metus elit in urna. Sed vehicula, nisi non luctus porttitor, lectus lectus luctus elit, nec cursus enim nisi vitae nisl. Suspendisse potenti. Donec quis mi nec eros tincidunt sodales. Pellentesque interdum sapien id ante dictum, at interdum odio volutpat. Ut eu sapien nec sapien placerat ultrices. Curabitur at nunc malesuada, posuere mi et, egestas est. Aliquam erat volutpat. Nam non purus ac urna facilisis pretium sit amet id velit. Fusce malesuada mauris id libero eleifend, id aliquet mi pharetra. Suspendisse ornare, ex non maximus fringilla, justo libero facilisis lorem, quis efficitur nisl ipsum vel tortor. Nam non purus ac urna facilisis pretium sit amet id velit. 3. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-AnthonyBiller.webp "Anthony Biller") Anthony Biller Director of New Business Development Vestibulum ante ipsum primis in faucibus orci luctus et ultrices posuere cubilia curae; Integer ut elit id lorem fermentum auctor non sit amet elit. Vivamus convallis euismod elit id vulputate. Integer id felis ac lacus dapibus ultrices. Proin id interdum tortor. Duis in justo neque. Sed vehicula tincidunt risus, non interdum lectus fermentum nec. Nullam vitae lorem a arcu eleifend tincidunt vitae eu nibh. Curabitur laoreet, purus et volutpat suscipit, felis libero hendrerit ipsum, a fermentum metus elit in urna. Phasellus lacinia, arcu non hendrerit ultricies, odio magna laoreet sem, a volutpat metus quam a felis. Nam varius fermentum nulla, eget auctor justo interdum id. Suspendisse potenti. Donec quis mi nec eros tincidunt sodales. Pellentesque interdum sapien id ante dictum, at interdum odio volutpat. Aenean in tempor enim, vitae laoreet mauris. Donec quis mi nec eros tincidunt sodales. Nullam id eros sit amet velit gravida auctor. - ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-EricBiller.webp "Eric Biller") Eric Biller Operations Manager Phasellus lacinia, arcu non hendrerit ultricies, odio magna laoreet sem, a volutpat metus quam a felis. Nam varius fermentum nulla, eget auctor justo interdum id. Suspendisse potenti. Donec quis mi nec eros tincidunt sodales. Pellentesque interdum sapien id ante dictum, at interdum odio volutpat. Aenean in tempor enim, vitae laoreet mauris. 3. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-HuanTran.webp "Huan Tran") Huan Tran Director of Quality Affairs Ut eu sapien nec sapien placerat ultrices. Curabitur at nunc malesuada, posuere mi et, egestas est. Aliquam erat volutpat. Nam non purus ac urna facilisis pretium sit amet id velit. Fusce malesuada mauris id libero eleifend, id aliquet mi pharetra. Suspendisse ornare, ex non maximus fringilla, justo libero facilisis lorem, quis efficitur nisl ipsum vel tortor. 3. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-NicklausMahasena.webp "Nicklaus Mahasena") Nicklaus Mahasena New Business Development Engineer Aliquam erat volutpat. Nam at libero at turpis tristique lacinia. Sed nec erat in elit scelerisque vehicula. Vivamus vitae nulla vitae elit tincidunt cursus in sit amet ex. Phasellus euismod libero a magna luctus, non pellentesque nunc consequat. Nulla facilisi. Cras vehicula, lorem a dapibus venenatis, quam enim convallis purus, vel pharetra est nisi non lorem. 3. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-AlexiosCampos.webp "Alexios Campos") Alexios Campos Material Control Aliquam erat volutpat. Nam at libero at turpis tristique lacinia. Sed nec erat in elit scelerisque vehicula. Vivamus vitae nulla vitae elit tincidunt cursus in sit amet ex. Phasellus euismod libero a magna luctus, non pellentesque nunc consequat. Nulla facilisi. Cras vehicula, lorem a dapibus venenatis, quam enim convallis purus, vel pharetra est nisi non lorem. 3. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/Intellitech-Team-DavidJiminez.webp "David Jiminez") David Jiminez Lead Cleanroom Technician Phasellus lacinia, arcu non hendrerit ultricies, odio magna laoreet sem, a volutpat metus quam a felis. Nam varius fermentum nulla, eget auctor justo interdum id. Suspendisse potenti. Donec quis mi nec eros tincidunt sodales. Pellentesque interdum sapien id ante dictum, at interdum odio volutpat. Aenean in tempor enim, vitae laoreet mauris. ### We welcome the opportunity to work with you ##### We support companies spanning the realm of R&D to GMP with a range of products and services. Call **1-727-914-7000** or [**contact us**](/contact-us/) to share your project, goals, and challenges. [ Contact Us ](/contact-us/) --- ### [Large Volume Filling](https://intellitech-inc.com/large-volume-filling/) **Published:** December 1, 2020 **Author:** craig **Content:** # Large Volume Filling ### i-FILL – Large Volume Filling (10ml – 100ml) The i-FILL pump is for fill volumes of 10ml to 100ml. The technology is ideally suited for water-like, high-value, sensitive product where product loss is costly and unacceptable. The pump is easily configured and controlled through a color touch-screen digital display. Fill profiles can be programmed to control foamy product or challenging product characteristics and saved as reusable recipes. The pump is not suited for highly viscous product. The pump is operated via the touch screen or foot pedal. ![large volume filling](https://intellitech-inc.com/wp-content/uploads/2020/12/pump-cutout.png "pump-cutout - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### This pump is validated and being used in regulated filling suites around the world. Validation support templates are available. The i-Fill is proven to deliver repeatable, precision dispensing over thousands of cycles. It outperforms peristaltic pumps with no risk of spallation or having to recalibrate for fill volumes trending out of tolerance. There is no dripping from the nozzle between dispenses. ### Request a Quote ##### Innovative solutions that are custom configured to meet your needs. Contact us today to build a custom liquid filling machine with tighter fill tolerances to suit you. [ Request a quote ](/request-a-quote/) ## Intellitech Products Many of our customers are involved in biologic drug/therapy/vaccine R&D and transitioning to GMP production and we, at Intellitech, believe we can best support those efforts by continuing to focus on manufacturing and improving the i-FILL family of precision liquid dispensing pump technology and single-use systems. #### Single Use Assemblies ### Single Use Assemblies Intellitech has unique experience in the design, development and manufacture of many assemblies used in BIO/PHARMA development and production. [Read More](https://intellitech-inc.com/single-use-assemblies/) #### Fluid/Cell Transfer Pump ### Fluid/Cell Transfer Pump The i-Fill® pump is proven effective to transfer live cells with little to no effect on the cells after varying tested periods of time. [Read More](https://intellitech-inc.com/fluid-cell-transfer-pump/) #### Precision Filling Pump ### Precision Filling Pump The i-Fill® delivers unmatched, repeatable dispense accuracy over thousands of dispenses for volumes of 100mcL to 100mL. [Read More](https://intellitech-inc.com/precision-filling-pump/) ### Large Volume Filling ### Large Volume Filling The i-FILL pump is for fill volumes of 100ml to multi liters. The technology is ideally suited for water-like, high-value, sensitive product where product loss is costly and unacceptable. [ Learn More ](/large-volume-filling/) ### Automated Tray Filling ### Automated Tray Filling This affordable fixture is an accessory to the i-FILL Micro that converts your process from manual filling to semi-automatic with ease and simplicity. [ Learn More ](/semi-auto-filling/) ### Closure Systems ### Closure Systems The i-CAP® Torque Unit provides automated tightening of container screw tops. [ Learn More ](/crimp-cap/) --- ### [Innovation Timeline](https://intellitech-inc.com/timeline/) **Published:** December 3, 2024 **Author:** craig **Content:** # Innovation Timeline ## A Legacy of Excellence ### From Groundbreaking Products to Cleanroom Expertise Explore our journey of innovation and growth. From the first i-FILL pump in 2002 to expanding cleanroom manufacturing in 2024, discover how Intellitech became a leader in precision dispensing and biopharma solutions. View our timeline to learn more about our milestones and evolution. ![](https://intellitech-inc.com/wp-content/uploads/2024/11/IntelliTech-Logo-stacked-2024.png "IntelliTech-Logo-stacked-2024 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ## Intellitech Product Innovation Timeline ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-Filler.webp) ##### 2002 Intellitech releases the first iteration of the i-FILL precision dispensing pumps. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-Filler.webp) ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-Capper-BackView.webp) ##### 2003 Intellitech releases the i-CAP family of container closure systems. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-Capper-BackView.webp) ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-ifs_left.webp) ##### 2004-2006 Intellitech releases the Intelli-Filler family of automatic and semi-automatic fill-finish machines. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-ifs_left.webp) ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-2006.webp) ##### 2006 Intellitech releases the i-FILL Micro and transitions into producing Single-Use Technologies for i-FILL pump heads, away from stainless steel. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-2006.webp) ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-OLD-iFILLMicro-XY.webp) ##### 2012 Intellitech develops and releases the XY tray filler as an accessory for semi-automated filling with the i-FILL Micro. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-OLD-iFILLMicro-XY.webp) ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-OLD-Cleanroom-DiagonalView.webp) ##### 2015 Intellitech relocated from Westminster, Maryland to St. Petersburg, FL to expand its custom single-use systems manufacturing space to offer Cleanroom assembly and Validation services for customers in Biopharma and Specialty Chemicals. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-OLD-Cleanroom-DiagonalView.webp) ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-Packaging-Inspection-Area-Picture.webp) ##### 2019 Intellitech's receives ISO9001:2015 certification for its Quality Management System. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-Packaging-Inspection-Area-Picture.webp) ![](https://intellitech-inc.com/wp-content/uploads/2025/01/intelitech-timeline-2020-2021.webp) ##### 2020-2021 Intellitech expands it's cleanroom manufacturing area. ![](https://intellitech-inc.com/wp-content/uploads/2025/01/intelitech-timeline-2020-2021.webp) ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-5MinuteMontagewScaleBar.webp) ##### 2023-2024 Intellitech collaborates with University of South Florida’s Biomedical Engineering Department to conduct comparison studies between the i-FILL and other pump technologies for impact on cell viability. ![](https://intellitech-inc.com/wp-content/uploads/2024/12/Intellitech-TL-5MinuteMontagewScaleBar.webp) ### An innovative manufacturer of single-use process components and assemblies, cell transfer bottles and manifolds for the Pharmaceutical, Life Sciences and Specialty chemical industries. [ View Our Services ](#) ### We welcome the opportunity to work with you ##### We support companies spanning the realm of R&D to GMP with a range of products and services. Call **1-727-914-7000** or [**contact us**](/contact-us/) to share your project, goals, and challenges. [ Contact Us ](/contact-us/) --- ### [iFILL Products](https://intellitech-inc.com/i-fill-products/) **Published:** November 18, 2024 **Author:** craig **Content:** # iFILL Products #### Unmatched Accuracy For Every Dispense ## Intellitech's i-FILL & i-FILL Micro Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Contact us for more info or a virtual demo. [ Contact Us ](/contact-us/) ![live cell transfer pump Cleanroom Assembly i-FILL i-FILL Micro](https://intellitech-inc.com/wp-content/uploads/2020/07/iFIll-Micro.png "iFIll-Micro - Intellitech Inc | Innovators of Single-Use Liquid Filling") ![](https://intellitech-inc.com/wp-content/uploads/2023/12/video-bkg.png "video-bkg.png - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Headline Coming Soon Intellitech’s i-FILL line of pumps delivers unmatched and repeatable dispense accuracy over thousands of dispenses for volumes from 100µL to 100mL. The i-FILL pumps utilize a single-use fluid path, available in both sterile and non-sterile conditions. These pumps are tailor-made for bench top, semi-automatic, aseptic filling applications. They can also be integrated into larger filling applications. ![I-FILL-Micro-Oct 2023-13](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/I-FILL-Micro-Oct-2023-13-qx8yolx7w52ykarjwejbunfgjw6s04qhvhhd6d6ws0.webp "I-FILL-Micro-Oct 2023-13") ### i-FILL Micro #### Accurate and Repeatable Small Volume Filling - Highly Accurate and Precise Dispensing - Qualified for Live-Cell Transfer [ Learn More ](/i-fill-micro/) ![Large i-FILL Picture](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/Large-i-FILL-Picture-qx8yox7a65iefmb62jeuokkzoin6khz9x1b6xoq6pc.webp "Large i-FILL Picture") ### i-FILL #### Accurate and Repeatable Large Volume Filling - Highly Accurate and Precise Dispensing [ Learn More ](/i-fill/) #### i-FILL Micro ### Accurate and Repeatable Small Volume Filling Highly Accurate And Precise Dispensing Qualified For Live-Cell Transfer [Learn More](/i-fill-micro/) #### i-FILL ### Accurate and Repeatable Large Volume Filling Highly Accurate And Precise Dispensing [Learn More](/i-fill/) ![](https://intellitech-inc.com/wp-content/uploads/2024/11/I-FILL-Interface-4.webp "I-FILL-Interface-4 - Intellitech Inc | Innovators of Single-Use Liquid Filling") #### A user-friendly interface allows the ability to quickly create recipes for different dispensing volumes or flow rates. Both the i-FILL Micro and the i-FILL are highly configurable for flow rates from 2 mL/min to 1 L/min. [ i-FILL Technical Specification Sheet ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-FILL-Technical-Specifications-Rev-4-31OCT2024.pdf) [ i-FILL Micro Specification Sheet ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-FILL-Micro-Technical-Specifications-Rev-4-31OCT2024.pdf) ## i-FILL Add-Ons #### Made to Fit Your Application #### i-FILL Footswitch ### i-FILL Footswitch #### Ergonomic Filling Over Many Dispenses [Learn More](#) #### XY Filling Tray (Future) ### XY Filling Tray (Future) #### Converting Tray Filling From Manual to Semi-Automated [Learn More](#) #### i-FILL Micro Pedestal ### i-FILL Micro Pedestal #### Headline Coming Soon [Learn More](#) ![iFILL-AddOns-XYFillingTray](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/iFILL-AddOns-XYFillingTray-qx8zmmox99nks7ci8ly7lkd2kyi1lqsqvvj1hwqxkg.webp "iFILL-AddOns-XYFillingTray") ### i-FILL Footswitch #### Ergonomic Filling Over Many Dispenses [ Learn More ](#) ![iFILL-AddOns-XYFillingTray](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/iFILL-AddOns-XYFillingTray-qx8zmmox99nks7ci8ly7lkd2kyi1lqsqvvj1hwqxkg.webp "iFILL-AddOns-XYFillingTray") ### XY Filling Tray (Future) #### Converting Tray Filling from Manual to Semi-Automated [ Learn More ](#) ![iFILL-AddOns-XYFillingTray](https://intellitech-inc.com/wp-content/uploads/elementor/thumbs/iFILL-AddOns-XYFillingTray-qx8zmmox99nks7ci8ly7lkd2kyi1lqsqvvj1hwqxkg.webp "iFILL-AddOns-XYFillingTray") ### i-FILL Micro Pedestal #### Headline Coming Soon [ Learn More ](#) --- ### [i-FILL Micro](https://intellitech-inc.com/i-fill-micro/) **Published:** November 12, 2024 **Author:** craig **Content:** # i-FILL Micro #### Accurate and Repeatable Small Volume Filling, Qualified for Cell Transfer ## i-FILL Micro - Small Volume Filling The i-FILL® Micro is a hybrid piston/diaphragm pump that delivers repeatable dispense accuracy for small fill volumes up to 15mL per piston stroke. It is also ideal for delicate product transfer. ![live cell transfer pump Cleanroom Assembly i-FILL i-FILL Micro](https://intellitech-inc.com/wp-content/uploads/2020/07/iFIll-Micro.png "iFIll-Micro - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### The i-FILL Micro Offers - Semi-automated R&D, Lab, or Production Filling - Fill volumes up to 15mL per stroke - No tubing spallation - Multiple dispensing and flow rate profiles that can be stored as recipes - Ease of operation with its user-friendly interface - Elimination of repetitive stress injuries from manual pipetting - Elimination cleaning and sterilization protocols with a single-use pump head - Self-priming - No dripping between dispenses - Ability to pump dry, eliminating Product Waste [ Contact Us About i-FILL Micro ](/contact-us/) #### Contact Us to Learn More About the i-FILL Micro [ Contact Us ](/contact-us/) ![](https://intellitech-inc.com/wp-content/uploads/2023/10/I-FILL-Interface-4-1024x788.jpg "I-FILL-Interface-4 - Intellitech Inc | Innovators of Single-Use Liquid Filling") #### A user-friendly interface allows users to easily adjust fill volumes, fill speeds, and flow rates. These settings can be saved into recipes to fit specific unit operations. [ i-FILL Micro Spec Sheet ](/resources/) [ ](https://intellitech-inc.com/wp-content/uploads/2024/11/i-fill-front-image1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/I-FILL-Oct-2023-4-scaled-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/2-days-MF-IF-1-Hour-BC-Adjusted-300x200-1.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/4-i-FILL-Cell-viability-after-2-hours-and-2-days.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/PrestoBlue-Assay-Picture.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6613.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2024/12/i-fill-micro-front-12-24.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6127.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6114.webp) [ ](https://intellitech-inc.com/wp-content/uploads/2025/01/Final-6119.webp) #### Intellitech collaborated with University of South Florida to study the i-FILL pump and a leading peristaltic pump for cell viability. 2 studies have been conducted to examine the application of the i-FILL Micro pumps for transporting live cells. The team conducted Trypan-blue cell viability experiments with sample volume suspensions. In the first study, NIH-3t3 mouse fibroblast cells were used. In the second study, human donor T-cells were used. In both studies, the cells were examined via live-cell imaging. The 2nd study also utilized Presto-blue assays as another method for measuring cell viability. In both studies, the results showed that the i-FILL Micro is capable for cell culture conditions during development and production. It is now qualified to be a viable alternative to the peristaltic pump. While the i-FILL pump has performed as a highly accurate dispensing pump, it is proven to be a highly capable cell transfer pump for both upstream and downstream cell culturing and bioprocessing, e.g. product transfer from a mixing vessel to filtration, from filtration to cell harvesting and transfer to either a finishing or a storage vessel. #### Interested in learning more? Please provide your contact information to receive an executive summary from one of the cell viability studies. Name(Required) First Last Email(Required) Your Business Name(Required) Your Business Website Message(Required) CAPTCHA Submit ## Intellitech Products Many of our customers are involved in biologic drug/therapy/vaccine R&D and transitioning to GMP production and we, at Intellitech, believe we can best support those efforts by continuing to focus on manufacturing and improving the i-FILL family of precision liquid dispensing pump technology and single-use systems. #### Single Use Assemblies ### Single Use Assemblies Intellitech has unique experience in the design, development and manufacture of many assemblies used in BIO/PHARMA development and production. [Read More](https://intellitech-inc.com/single-use-assemblies/) #### Fluid/Cell Transfer Pump ### Fluid/Cell Transfer Pump The i-Fill® pump is proven effective to transfer live cells with little to no effect on the cells after varying tested periods of time. [Read More](https://intellitech-inc.com/fluid-cell-transfer-pump/) #### Precision Filling Pump ### Precision Filling Pump The i-Fill® delivers unmatched, repeatable dispense accuracy over thousands of dispenses for volumes of 100mcL to 100mL. [Read More](https://intellitech-inc.com/precision-filling-pump/) --- ### [Contact Us](https://intellitech-inc.com/contact-us/) **Published:** December 29, 2020 **Author:** craig **Content:** # Contact Us ### Please fill out this form and we will reply to you as soon as possible. Note: Your information is protected and used solely by Intellitech to contact you regarding your interest in single-use systems. Under no circumstance is your contact information shared with any other entity. Email This field is for validation purposes and should be left unchanged. Name(Required) First Last Email(Required) Phone Best Time To Reach You:Day of the Week & Time of Day Interested in:(Required) Precision Liquid Filling Custom Single Use System(s) Validation Services Cell Transfer Pump Quality Inquiries Request a Quote Ask an Engineer Comment / Question: Submit ![.](https://intellitech-inc.com/wp-content/uploads/2025/06/intellitech-logo-stacked-2025.png "intellitech-logo-stacked-2025 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Contact Intellitech - 11801 28th St. N, Unit #5 Saint Petersburg, Florida 33716 - [ 727-914-7000 ](tel:727-914-7000) [ Facebook ](https://www.facebook.com/Intellitechinc/) [ Twitter ](https://twitter.com/i_fill4u) [ Youtube ](https://www.youtube.com/user/intelliTECHinc) [ Linkedin ](https://www.linkedin.com/company/intellitech-inc-?trk=tyah&trkInfo=clickedVerticalcompanyclickedEntityId1087786idx2-5-6tarId1468357028816tasintellitech) - [ ISO 9001:2015 Certified by NQA ](https://intellitech-inc.com/wp-content/uploads/2022/12/Intellitech-NQA-ISO-9001-Certificate-18396_12-9-22.pdf) --- ### [Cleanroom Assembly & Packaging Service](https://intellitech-inc.com/cleanroom-assembly-packaging/) **Published:** November 19, 2024 **Author:** craig **Content:** # Cleanroom Assembly & Packaging Service ## Cleanroom Environments for High Quality Single-Use System Manufacturing. Intellitech’s Cleanroom Assembly and Packaging Services puts our customers at ease, maintaining highly controlled environments and processes for single-use assembly and packaging that meet strict sterility and bioburden requirements. ![](https://intellitech-inc.com/wp-content/uploads/2024/11/icon-outlined-Cleanroom-Assembly-Packaging-Services.webp "icon-outlined-Cleanroom-Assembly-Packaging-Services - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Ensuring Excellence ISO-certified cleanrooms are important for single-use systems production, especially when these systems will be used in biopharmaceutical manufacturing. Intellitech maintains ISO7-Certified cleanrooms through processes that ensure optimal environmental conditions, personnel behaviors, and controlled transferring activities. These processes ensure that our cleanroom environments remain controlled while contaminants and particulates are kept to a minimum. This guarantees high quality products for our customers. ### Trusted Assembly & Packaging Our Cleanroom Technicians are trained in assembling and packaging single-use systems, ensuring that they are handled, sealed, and delivered in compliance to GMP. With experience in producing single-use systems for large biopharmaceutical companies, Intellitech is qualified provider of reliable and efficient cleanroom assembly and packaging. ### Testing & Validation Service #### Intellitech works with an accredited third-party testing lab to perform relevant testing and validation on your single-use systems. [ Read More ](/testing-validation/) ## Explore Intellitech's Services #### Intellitech Covers The Spectrum To Support Customers From R&D To GMP. [![](https://intellitech-inc.com/wp-content/uploads/2024/11/design-engineering-icon.webp "design-engineering-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/design-engineering/)### [Design & Engineering Services](/design-engineering/) [ Learn More ](/design-engineering/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/prototyping-fabrication-icon.webp "prototyping-fabrication-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/prototyping-fabrication/)### [Prototyping & Fabrication Services](/prototyping-fabrication/) [ Learn More ](/prototyping-fabrication/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/assembly-packaging-icon.webp "assembly-packaging-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/cleanroom-assembly-packaging/)### [Cleanroom Assembly & Packaging Services](/cleanroom-assembly-packaging/) [ Learn More ](/cleanroom-assembly-packaging/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/testing-validation-icon.webp "testing-validation-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/testing-validation/)### [Testing & Validation Services](/testing-validation/) [ Learn More ](/testing-validation/) --- ### [About](https://intellitech-inc.com/about/) **Published:** December 1, 2020 **Author:** craig **Content:** # About ## Over 25 Years As An innovative manufacturer ### Young by some standards, yet having proven the test of time by entrepreneurial standards. Like many entrepreneurial startups, Intellitech began as Biller’s Design Service in the basement of Andy and Barb Biller’s home. The company delivered drafting, design and documentation services for client companies such as Northrop Grumman. During the early years, Andy brought on young interns from the Carroll County Technology Center to begin their careers and gain experience. Jamie G., Jamie L., Brent B., Ben T. and many others would all go on to pursue additional education and careers with companies including Northrop Grumman, AAI Corporation, General Dynamics, and York International. ![.](https://intellitech-inc.com/wp-content/uploads/2025/06/intellitech-logo-stacked-2025.png "intellitech-logo-stacked-2025 - Intellitech Inc | Innovators of Single-Use Liquid Filling") Like many entrepreneurial startups, Intellitech began as Biller’s Design Service in the basement of Andy and Barb Billers home. The company delivered drafting, design and documentation services for client companies such as Northrop Grumman. During the early years, Andy brought on young interns from the Carroll County Technology Center to begin their careers and gain experience. Jamie G., Jamie L., Brent B., Ben T. and many others would all go on to pursue additional education and careers with companies including Northrop Grumman, AAI Corporation, General Dynamics, and York International. ## Intellitech Explored And Exploited Opportunities For Growth in Innovative Manufacturing Expansion as an AutoCAD software reseller and training source supported building design expertise in 3-D modeling and automated design tools. Customer requests drove the company to move from design into first-article prototype and initial production of custom, automated systems. From initial prototypes, the company began to build expertise in precision liquid filling and has continued to build this technology niche since early 2000. Today, Intellitech manufactures bench-top precision liquid filling systems, registered as the i-FILL® family of pumps. They deliver unmatched repeatability and accuracy for liquid filling volumes up to 100mL. Both the [i-FILL ](/i-fill/)and [i-FILL Micro](/i-fill-micro/) have been qualified for transferring delicate product such as live cells. Both the i-FILL pump models feature a single-use fluid path, ideally suited to the life science industry to ensure product sterility and reduce the need for time-consuming cleaning protocols. ### An Innovative, Full-Service Manufacturer of Single-Use Systems and Precision Dispensing Pumps for Biopharma. [ View Our Services ](/our-services/) [ View Our Products ](/products/) #### In 2015, Intellitech moved from Westminster, Maryland to St. Petersburg, Florida, allowing expansion of manufacturing and cleanroom assembly space to better serve its growing global customer base. In 2019, NQA (an accredited ISO registrar) recommended registration of Intellitech’s Quality Management System to [ISO 9001:2015](https://intellitech-inc.com/wp-content/uploads/2022/12/Intellitech-NQA-ISO-9001-Certificate-18396_12-9-22.pdf) under the scope of: design, development, manufacture, assembly, packaging, sales and distribution of standard and custom single-use fluid path assemblies primarily used in the life science (bio/pharma) and specialty chemical industries. In 2020, a NQA surveillance audit revealed no major or minor observations – a rare event after a challenging year contending with an international pandemic and economic uncertainty. Intellitech’s quality-driven culture performs at the highest level. ### We welcome the opportunity to work with you ##### We support companies spanning the realm of R&D to GMP with a range of products and services. Call **1-727-914-7000** or [**contact us**](/contact-us/) to share your project, goals, and challenges. [ Contact Us ](/contact-us/) ## Intellitech Product Innovation Timeline ##### 2002 i-FILL family of precision dispensing pumps. ##### 2003 i-CAP family of container closure systems. ##### 2006 Disposable Kits for i-FILL family of pumps. ##### 2012 X-Y Tray filler developed as an accessory to the i-FILL family of pumps. ##### 2015 Cleanroom & Validation services for the SUT, For the Pharma, Life Sciences and Special Chemicals industries. --- ### [Design & Engineering Service](https://intellitech-inc.com/design-engineering/) **Published:** November 19, 2024 **Author:** craig **Content:** # Design & Engineering Service ## Custom Single-Use Designs, Made Simple. Intellitech’s Design & Engineering Service makes it easy to get a custom single-use system design that matches our customer’s requirements. ![](https://intellitech-inc.com/wp-content/uploads/2024/11/icon-outlined-Design-Engineering-Services.webp "icon-outlined-Design-Engineering-Services - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Design Bioprocessing requirements can be different from manufacturer to manufacturer in the biopharma industry. At Intellitech, we support customers in the R&D phase to design, develop, and document elements of the Design History File. Capturing the following elements ensures that the design is tailored to the customer’s application: - Requirements and Specification - Feasibility - Risk Analysis - Drawings - Bill of Materials - Design Reviews - Method of Manufacture - Product Packaging and Labeling To reduce the cost of investment, customers take advantage of using Intellitech’s design infrastructure tools including Solidworks 3D modeling, PDM (Product Data Management) vault and CAM software. PDM keeps track of file revision history, acting as a method of capturing and controlling design changes. ### Prototyping & Fabrication Service #### Upon Initial Review and Approval, Intellitech can Transition into Creating a Prototype of the Design to Conduct Initial Functional Testing and Provide Changes and Feedback. [ Read More ](/prototyping-fabrication/) ## Explore Intellitech's Services #### Intellitech Covers The Spectrum To Support Customers From R&D To GMP. [![](https://intellitech-inc.com/wp-content/uploads/2024/11/design-engineering-icon.webp "design-engineering-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/design-engineering/)### [Design & Engineering Services](/design-engineering/) [ Learn More ](/design-engineering/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/prototyping-fabrication-icon.webp "prototyping-fabrication-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/prototyping-fabrication/)### [Prototyping & Fabrication Services](/prototyping-fabrication/) [ Learn More ](/prototyping-fabrication/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/assembly-packaging-icon.webp "assembly-packaging-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/cleanroom-assembly-packaging/)### [Cleanroom Assembly & Packaging Services](/cleanroom-assembly-packaging/) [ Learn More ](/cleanroom-assembly-packaging/) [![](https://intellitech-inc.com/wp-content/uploads/2024/11/testing-validation-icon.webp "testing-validation-icon - Intellitech Inc | Innovators of Single-Use Liquid Filling")](/testing-validation/)### [Testing & Validation Services](/testing-validation/) [ Learn More ](/testing-validation/) --- ### [Request A Quote](https://intellitech-inc.com/request-a-quote/) **Published:** December 29, 2020 **Author:** craig **Content:** # Request A Quote Facebook This field is for validation purposes and should be left unchanged. Name(Required) First Last Email(Required) Phone Best Time To Reach You:Day of the Week & Time of Day Interested in:(Required) Precision Liquid Filling Custom Single Use System(s) Validation Services Cell Transfer Pump Quality Inquiries Request a Quote Ask an Engineer Comment / Question: Submit ![.](https://intellitech-inc.com/wp-content/uploads/2025/06/intellitech-logo-stacked-2025.png "intellitech-logo-stacked-2025 - Intellitech Inc | Innovators of Single-Use Liquid Filling") ### Contact Intellitech - 11801 28th St. N, Unit #5 Saint Petersburg, Florida 33716 - [ 727-914-7000 ](tel:727-914-7000) [ Facebook ](https://www.facebook.com/Intellitechinc/) [ Twitter ](https://twitter.com/i_fill4u) [ Youtube ](https://www.youtube.com/user/intelliTECHinc) [ Linkedin ](https://www.linkedin.com/company/intellitech-inc-?trk=tyah&trkInfo=clickedVerticalcompanyclickedEntityId1087786idx2-5-6tarId1468357028816tasintellitech) - [ ISO 9001:2015 Certified by NQA ](https://intellitech-inc.com/wp-content/uploads/2022/12/Intellitech-NQA-ISO-9001-Certificate-18396_12-9-22.pdf) ---