Insource or Outsource cGMP Batch Documentation (WS18)
- Date:
- 30 April 2019
- Time:
- -
- Available Seats:
- 24
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.
