ACT EU PA04 – Multi-stakeholder Workshop on ICH E6 R3
Date: September 25, 2023
As part of the Accelerating Clinical Trials in the EU (ACT EU) multi-annual workplan 2022-2026 and acknowledging the important role of ICH E6 as the global regulatory guideline for GCP, a multi-stakeholder workshop on ICH E6 R3 public consultation was organised by ACT EU Priority Action 4 (PA4).
If you weren’t able to participate in the workshop, a recording is available here.
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https://acdmglobal.org/wp-content/uploads/2022/04/ACDM_FDA_DHT.pdf