Biopharmaceutical Testing Services | Charles River

viral & TSE clearance studies 

laboratory for performing viral and TSE clearance studiesStudies designed to demonstrate the capacity of a manufacturing process to inactivate or remove viruses and transmissible spongiform encephalopathy (TSE) agents are required by regulatory authorities for animal- or human-derived products (e.g., cell cultures) as an integral part of any submission report prior to administration of the product in humans.

At Charles River Biopharmaceutical Services (BPS), we have expert scientists in both the US and Europe who have more than 20 years of experience in supporting clients throughout the design and performance of viral and TSE clearance studies. Using a customized approach, we are able to provide technical advice and regulatory support to ensure that a successful and cost-effective program is established and reports are generated to meet your deadlines. All process validation/viral clearance studies are performed according to ICH Q5A and European, US, Japanese and WHO regulatory guidelines.  

Our new Cologne, Germany-based center of excellence for viral clearance has the ability to handle up to five studies in parallel. We provide extended services, including performance of almost all downscaled process steps (e.g., virus-retentive filtration, inactivation, chromatography), which means more flexibility and improved timelines for clients. Click here to view a tour of the Cologne facility.

Capabilities

  • cGMP- and GLP-compliant viral clearance studies
  • Qualified GE AKTA Purifier and Explorer chromatography systems
  • Pilot lyophilization machine
  • Performance of most downscaled process steps according to client's protocols
  • Downscale service
  • Human and animal viruses available as high-titer stocks (>107 PFU/mL/>107 TCID50/mL)
  • Infectivity assays performed in real time
  • Large-volume assay format available to improve LRV claims
  • Q-PCR assays available
  • Supporting Microbiology and Molecular and Cellular Biology services
  • Regulatory advice and consulting
  • Available to conduct seminars at client sites
  • Database of more than 2000 GLP studies

 

Product Experience

  • Monoclonal antibodies
  • Recombinant proteins
  • Transgenic products
  • Tissue-derived products
  • Blood-derived products
  • Medical devices


To check which of our BPS facilities perform viral and TSE clearance studies, click here. For additional information
, contact us at askcharlesriver@crl.com or 1.877.CRIVER.1.

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For more information, contact us at:

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

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Manager International Tax Wilmington, MA

Charles River Laboratories, Inc.