Biopharmaceutical Development Services | Charles River

biopharmaceutical services 

 
 

Delivering a biologic to the market can be a challenging, financially demanding and time-consuming process. Robust safety data, timely reporting and rigorous attention to quality and detail are critical factors in the successful development of a biologic. Charles River Biopharmaceutical Services (BPS) delivers client-focused solutions for the specific testing and manufacturing requirements of your biologic.

BPS follows international regulatory guidelines for testing and clinical-scale manufacturing of biologics. The assays provided range from cell characterization and process validation studies through to stability and product release testing. Manufacturing services include cell banking, storage, fill and finish, and viral vaccine and antisera production.

Our global footprint now includes sites in both Erkrath and Cologne in Germany, which complement our existing facilities in Malvern, PA; Edinburgh, UK; and Ballina, Co. Mayo, Ireland. Furthermore, to address the growing Asian market, BPS has agents in Japan (LSG Corporation), India (Zelle Biotechnology Private Limited), Korea (Sartorius Korea Biotech) and Taiwan (LifeOptimal Technology, Inc.). As a global organization, BPS can provide you with more flexibility, experience and expertise in multiple regulatory environments to accelerate the development of your biologic, enabling you to get your product to market faster.

Discover the full range of Charles River Products and Services

For more information please call:

1.877.CRIVER.1 (1.877.274.8371)
askcharlesriver@crl.com

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This webinar focused on the regulatory requirements for viral clearance studies as well as the influence of various other factors relevant to designing these studies.

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Charles River Laboratories, Inc.