EMA – Publication of the presentation material and video recordings of the ACT EU workshop on ICH E6 R3 (principles and Annex 1) held the 19 and 20 February 2025
The workshop aimed to engage all stakeholders of ICH E6 R3, including but not limited to patients, healthcare professionals, including investigators, regulators, service provider, ethics committees members industry and academia.
The objectives of this workshop were to:
- provide an overview of the major changes in the ICH E6(R3) guideline, including changes from the draft version of the ICH E6(R3) guideline that was published for public consultation;
- highlight key concepts for adaptation of Good Clinical Practice to recent developments in trial design, organisation and technology, and how these will help to future-proof the guideline;
- enable discussion with stakeholders on the implementation of ICH E6(R3).
The EMA published all the presentation materials and the video recordings of the event on its Website.
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vroby (26 mars 2025). EMA – Publication of the presentation material and video recordings of the ACT EU workshop on ICH E6 R3 (principles and Annex 1) held the 19 and 20 February 2025. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/13knc





