The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) E6 guideline for Good Clinical Practice (GCP) is the global standard for designing, conducting, recording, and reporting clinical trials involving human participants. It ensures the rights, safety, and well-being of trial participants while maintaining the integrity and credibility of clinical trial data [1]. The transition from ICH E6(R2) to ICH E6(R3) introduces significant updates to address the evolving landscape of clinical research, emphasizing flexibility, risk-based approaches, and the integration of digital technologies. This article explores the key changes in the final version of ICH E6(R3) and provides actionable insights for clinical trial sites to adapt effectively.

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Cross-Specialty

Relevant across 8 specialties.

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$30 – $40

$30 · $40

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Listed by the provider · about.citiprogram.org

On-demand / recorded video
Credit · Up to 2 credits
MOC · Up to 2 points
$30–40

Released

Jan 1, 2026
Last day to claim credit

Jan 1, 2027 3 months left

ICH Guideline for Good Clinical Practice E6(R3) 2026

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