Insource or Outsource cGMP Batch Documentation (WS18)

29 April 2019
Available Seats:

Reviewing manufacturing and packaging batch records for release of investigational product is a integral part of the clinical supply chain.   The decision on whether to retain the responsibility at the sponsor company or to fully/ partially outsource can be challenging.  This session will look at the benefits and risks of outsourcing this key quality activity and how to appropriately manage communication of delegated responsibilities. 

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