A CDMO's Perspective on the Development of Bioprocesses for Clinical Manufacturing Success

BPI Contributor

December 20, 2019

20 Min View
A CDMO's Perspective on the Development of Bioprocesses for Clinical Manufacturing Success

Date: Dec 20, 2019

Duration: 20 Min

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This webcast features: Nigel Shipston, Director, Program Design, FUJIFILM Diosynth BiotechnologiesFDB_12-17-19-300x159.png

A strategy for the development and scale of bioprocesses should be assessed at the earliest of stages. There are different challenges depending on the molecule and expression system. This webinar is designed to address some of the areas of consideration for successful development of bioprocesses for biologics and gene therapies. At the end of this webinar, you will be able to do a self-assessment to answer some critical questions:

  • Is the product/clinical development plan defined?

  • How do we create a cell line?

  • Is this the right expression system?

  • How much focus should we put on analytics?

  • Should I do more before looking for a CDMO for early clinical development?

Watch the recorded webcast below.

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