Successfully navigate the EU Clinical Trials Regulation, and more.
13th April 4pm CET
- Expectations and responsibilities of UK and EU QPs
- Impact of the EU Clinical Trials Regulation and its challenges
- Clarity on labelling requirements, especially for Auxiliary Medicinal Products
- How to ensure supply continuity across Europe
- The QP oversight process when importing into the UK
- Auditing in a post-COVID world
- Impact of new direct-to-patient distribution models
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16 February 2023