Service Provider Life Cycle Management - Essential Steps to Achieving Quality and Compliance
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More information20th January 2025
EMA - ICH E6(R3) Revision Workshop
The Accelerating Clinical Trials in the EU (ACT EU) initiative is organising a public workshop on the ICH E6 R3 revision on 19-20 February 2025 to support stakeholders in the implementation of the revised guideline. The registration is now closed but you can follow the live broadcast on the event page.
Annex 2 of the guideline is being developed in parallel. It provides additional GCP considerations focusing on examples of trials that incorporate decentralised elements, pragmatic elements and/or real-world data. A draft of Annex 2 is currently under public consultation, concluding on 28 February 2025.