Successfully navigate the EU Clinical Trials Regulation, and more.

Topics include:

  • Expectations and responsibilities of UK and EU QPs
  • Impact of the EU Clinical Trials Regulation and its challenges
  • How to ensure supply continuity across Europe
  • The QP oversight process when importing into the UK
  • Auditing in a post-COVID world
Register now

Meet the Speakers

Naomi Wilmer

QA Manager and QP at Thermo Fisher Scientific

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Join Qualified Persons (QP) experts from the UK and EU for a lively Q&A that looks back on the impact of the EU Clinical Trials Regulation and offers insights into the role of the QP and QP release.

Register now for forward-looking insights!

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