The latest edition of the EMA Clinical Trials Information System (CTIS) Newsletter provides insights on clinical trials topics. Of particular interest to HSRAA members is that the Accelerating Clinical Trials (ACT) EU programme is organising a series of workshops on the third revision of the ICH guideline on Good Clinical Practice (GCP), known as ICH E6 (R3). The ICH E6 (R3) guideline describes the responsibilities and expectations of all stakeholders in the conduct of clinical trials, and covers monitoring, reporting, and the archiving of trials.
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