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The pharmaceuticals industry requires exceptional hygiene, accuracy, and compliance at every stage of production. Pumps are used across a wide range of pharmaceutical processes—from transferring sterile ingredients to managing precision dosing and packaging. Whether in a GMP-certified plant or a cleanroom laboratory, efficient and sanitary pump systems are critical to maintaining product integrity, consistency, and traceability.

At the heart of fluid handling in the pharmaceuticals industry is the need for equipment that meets stringent standards, including FDA, USP Class VI, and EHEDG certifications. Pump selection must reflect the specific demands of each process, with reliability, validation support, and low-shear performance all playing vital roles.

Pharmaceuticals Industry Key Applications

1. Ingredient Transfer

The pharmaceuticals industry involves the careful handling of active pharmaceutical ingredients (APIs), excipients, and solvents. These materials must be transferred hygienically and without cross-contamination. Peristaltic, diaphragm, and magnetic drive pumps are commonly selected for their seal-less operation, ease of cleaning, and compatibility with sterile or aggressive fluids.

Maintaining a closed, contamination-free transfer system is especially important in cleanroom environments. These pump technologies help preserve ingredient quality while supporting validation and traceability.

2. Dosing and Metering

Accurate metering of ingredients, from active substances to pH adjusters, is essential in pharmaceutical production. Metering pumps offer precise, repeatable flow control, enabling consistency across both batch and continuous processes.

For the pharmaceuticals industry, even microflow rates must meet narrow tolerances. These dosing systems reduce waste, ensure formulation integrity, and help manufacturers meet regulatory expectations.

3. Biopharmaceutical and Aseptic Processing

In vaccine production, cell culture handling, and other biotech-related applications, pumps must operate with extremely low shear. These processes are highly sensitive, and any mechanical disruption can damage fragile biological materials or compromise yield.

Sanitary pumps designed for the pharmaceuticals industry support aseptic conditions, often in single-use setups. These systems simplify cleaning, reduce turnaround times, and align with GMP best practices.

4. CIP and SIP Cleaning Cycles

Clean-in-Place (CIP) and Sterilise-in-Place (SIP) systems are critical to maintaining hygiene in the pharmaceuticals industry. These processes rely on pumps to circulate hot water, cleaning agents, and steam through production equipment without disassembly.

Sanitary centrifugal and diaphragm pumps are often used for their ability to withstand high temperatures and chemical exposure. This ensures repeatable, validated cleaning cycles that support Good Manufacturing Practice (GMP) compliance as required in regulated pharmaceutical environments.

5. Filtration and Purification Processes

Pumps are essential to the downstream stages of pharmaceutical manufacturing, where fluids are passed through filters, chromatography columns, or purification membranes. These stages demand steady, pulsation-free flow to protect product yield and maintain separation accuracy.

In the pharmaceuticals industry, systems must operate gently and efficiently to avoid foaming, disruption, or loss of sensitive materials. Magnetic drive or peristaltic pumps are often preferred for these applications.

6. Filling and Packaging Lines

Final product packaging requires ultra-precise fluid handling to fill vials, syringes, blister packs, or bottles. Pumps must maintain strict hygiene, air-free delivery, and repeatable accuracy to meet cleanroom and sterility requirements.

In sterile fill-finish environments, pumps used in the pharmaceuticals industry need full validation support, traceable materials, and minimal maintenance demands to reduce downtime and risk of contamination.

How Tomlinson Hall Can Help?

With decades of experience supporting pharmaceutical manufacturing and processing, Tomlinson Hall offers proven solutions for every stage of fluid handling. We understand the regulatory, hygienic, and operational requirements unique to the pharmaceuticals industry and deliver pump systems that meet the highest standards of reliability and compliance.

We provide expert support for:

  • Precision dosing and aseptic transfer applications
  • Compliance with GMP, FDA, and USP Class VI requirements
  • Validated pump technologies for cleanroom and sterile zones
  • Efficient CIP/SIP integration for reduced downtime
  • Ongoing technical support and lifecycle maintenance

Looking for dependable pumping solutions for pharmaceutical production? Get in touch with our expert team today.

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