Our Virus Assay Development, qualifies and validates product specific, EP and USP analytical methods for use as in-process controls or release assays either as part of a development and manufacturing project, or as a stand-alone service.

Vibalogics offers a full analytical method development and analysis package tailored to virus based products and complimenting its manufacturing services. We provide a comprehensive virus assay development service, which not only covers product development and manufacturing, but also in-process, bulk intermediate and final product release analysis.

We believe that a full tool kit of assays should be available for our customers to choose from, which is why we have selected and audited a number of third party testing facilities to provide specific services that would not be cost effective for you if we performed them. However, all interactions with these facilities are managed by Vibalogics to keep the communication network simple and effective.

Our Virus Assay Development features…

  • A comprehensive list of assays for identity, potency, purity and safety
  • Assay development or transfer of existing assays to our facility for use as in-process or release tests
  • Qualification or validation based on EP or USP or assay specific specifications
  • Selected third party testing facilities audited and approved by Vibalogics to benefit our customers

All GMP assays at Vibalogics are performed to SOPs to ensure the highest level of reproducibility and confidence in the results obtained.

Our Assay development and testing packages are available as a stand-alone service, so why not speak to us today to find out how we can help you with your analytical testing requirements.

For more information regarding our Virus Assay Development & Testing services, contact us today on +49 4721 565 400 or email contact@vibalogics.com