Achieving precision, safety and compliance in biopharmaceutical manufacturing requires reliable, high-performance solutions. From fluid management and filtration to sealing and single-use technologies, innovative process control systems help enhance product integrity, accelerate drug development and meet stringent industry standards. With cutting edge solutions designed for scalability and efficiency, manufacturers can optimise bioprocessing workflows while ensuring the highest levels of purity and performance.
Find out more about Parker's biopharma processing capabilities below.
Bioprocessing Applications
Cell Culture
Harvesting
Buffer Preparation
Purification and Concentration
Bulk Fill
Freezing
Final Fill
PUPSIT
Browse our Bioprocessing Technologies
Single-Use Solutions
Parker utilises the latest technologies and extensive engineering and process expertise to advance bioprocessing with our PureTain® single-use solutions.
Bioprocess Automation
The use of automation in running complex single use processes has many benefits including improving process control and consistency, increasing speed, and reducing human error deviations.
Filtration
From clarification and bioburden reduction to sterile filtration and Mycoplasma removal, Parker offers a range of liquid and gas filters for all your filtration requirements. Filters can be incorporated into our SciLog® single-use systems to enhance process control and increase productivity.
Single-Use Sensing
Parker’s single-use sensors for pressure, temperature and conductivity measurement enhance bioprocess control and safety making them fundamental for monitoring critical applications such as virus filtration, ultrafiltration and diafiltration and bulk drug dispense.
Interactive
Bioprocessing Solutions
Parker products and complete solutions for biopharmaceutical applications ensure high performance of the fluid control and filtration systems, maximising uptime and productivity. They are designed to meet the requirements of next generation Bioprocessing
Featured Products
Scilog Fd Automated Filtration And Dispense System
Cold Chain Transportation And Storage Containers
Propor Mr Mycoplasma Removal Filters
Propor Sg Sterilizing Grade Pharmaceutical Filters
Propor Hc High Capacity Sterilizing Grade Filters
Manifold Systems For Biopharma Applications
Free Resources
Three Ways to Successfully Scale-Up
When developing a biopharmaceutical manufacturing process, an R&D or development team may fall into the trap of developing a process in the lab which is difficult to scale up for production volumes. Read how to avoid delays and additional development costs.
Application of Pre-Use Post Sterilisation Integrity Testing
The latest revision of EU GMP Annex 1: Manufacture of Sterile Medicinal Products (August 2023) included PUPSIT as a default requirement for manufacturers using filtration to sterilize their final product. Discover the considerations and challenges for the incorporation of PUPSIT into your processes.
Demystifying Extractables Testing
The increased focus by biomanufacturers on smaller patient populations is driving the adoption of technologies that can improve flexibility and process efficiency while also lowering overall costs. As a result, the application of single-use technology (SUT) is growing rapidly.
Improving Final Fill Processes and Addressing Annex 1 Requirements
Explore the evolving role of single-use systems in addressing critical challenges in final fill processes and meeting stringent regulatory requirements. Learn how Parker´s PureTain® solutions are reshaping processes, enhancing efficiency, and ensuring sterility, while aligning with regulatory standards.
Videos & Webinars
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Literature
Biopharmaceutical Industry Overview Guide
White Paper: Three ways to Successfully Scale-up
White Paper: Automation in Single-use
White Paper: Preventing Mycoplasma Contamination
White Paper: Demystifying Extractables Testing
White Paper: Implementation of Single-use
White Paper: Single-use-The next Five Challenges