The EU Clinical Trials Regulation no. 536/2014 became effective on 31 January 2022 and the first approved trials are now showing up in CTIS. Nevertheless, planning ahead for a successful submission and knowing what to expect from the new system can be a challenge.

  • Are you wondering when you should transition your ongoing trial to the EU CTR?
  • Whether you can switch from the trial-centric approach to the organisation-centric approach?
  • How and to whom to submit your safety reports under the EU CTR?

Just follow the link to this 30' session.

Details
  • May 12, 2022 @ 4:00 pm
  • Switzerland
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Location

Webinar - Lausanne, Switzerland

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