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The pharmaceutical industry demands the highest levels of hygiene, precision, and reliability from its fluid handling systems. Pumps are used throughout production—from transferring active ingredients to sterile dosing and packaging—where accuracy, traceability, and compliance are critical. Every stage must support cleanroom standards and Good Manufacturing Practice (GMP), making pump selection a key factor in process integrity and product safety.

Key Applications

1. Ingredient Transfer
Active pharmaceutical ingredients (APIs), solvents, and excipients must be transferred hygienically and without contamination. Peristaltic, diaphragm, and magnetic drive pumps are often chosen for their seal-less design, cleanability, and ability to handle aggressive or sterile fluids.

2. Dosing and Metering
Accurate dosing of liquid components is essential in both batch and continuous processes. Metering pumps provide precision control over flow rates, supporting consistent formulations and adherence to strict production specifications.

3. Biopharmaceutical and Aseptic Processing
In biotech and sterile drug manufacturing, pumps must maintain purity and protect sensitive biological materials. Low-shear, sanitary pumps support applications such as vaccine production, cell culture transfer, and filtration stages, often within single-use systems.

4. CIP and SIP Cleaning Cycles
Clean-in-Place and Sterilise-in-Place systems are standard in pharmaceutical plants. Pumps circulate cleaning agents and steam through production equipment without dismantling, ensuring full hygiene between production runs.

5. Filtration and Purification Processes
During downstream processing, pumps must deliver consistent flow through filters, chromatography columns, or other purification equipment. Smooth, pulsation-free operation is vital for preserving product yield and purity.

6. Filling and Packaging Lines
Final product filling into vials, bottles, or blister packs requires ultra-precise and hygienic pumps. These systems must operate without introducing air, bubbles, or contamination, especially in sterile fill-finish environments.

Industry Demands

  • Ultra-Clean Design: Pumps must meet FDA, USP Class VI, and EHEDG standards.

  • Traceability: Materials and components must be fully documented for GMP compliance.

  • Low Shear: Gentle pumping preserves biological activity and product structure.

  • Validation Support: Equipment must be compatible with qualification and validation protocols.

How Tomlinson Hall Can Help?

With over a century of experience in pump distribution and engineering solutions, Tomlinson Hall & Co Ltd supports the pharmaceutical industry with pump systems designed for high-purity, hygienic, and regulated environments. As a distributor for leading global pump manufacturers, we offer technologies trusted across pharmaceutical and biotech applications.

Our in-house team of technical experts can assist with:

  • Pump selection and specification for APIs, solvents, and aseptic processes

  • FDA- and GMP-compliant hygienic pump solutions

  • On-site consultations and troubleshooting

  • Bespoke pump builds and modifications

  • Full aftersales support, including servicing and repairs

Whether you’re manufacturing high-volume generics or niche biologics, Tomlinson Hall delivers reliable, cleanroom-ready pump solutions built for pharmaceutical excellence.

Need help finding the right pump for your pharmaceutical process?
Get in touch with our team today—we’re here to help.