Friday 19th June 2026 13:00 - 14:00 (BST)
The revision of ICH-GCP E6(R3) marks an important evolution in the framework guiding global clinical research. As clinical trials become increasingly complex and technology-driven, the updated guideline introduces a more flexible and risk-based approach while maintaining the highest standards of patient safety and data integrity.
This 60-minute masterclass will provide those working in medical and clinical functions a clear and practical overview of the revised framework and the thinking behind the update. Attendees will gain insight into how the new guideline aims to support modern clinical trial delivery while strengthening quality management across the research lifecycle.
Nelle Stocquart, Clinical Research & GCP Training Specialist, will explore the key differences between ICH-GCP E6(R2) and E6(R3), highlighting the updated principles, broader scope, and the evolving responsibilities of stakeholders involved in clinical research.
The session will also examine the international implementation landscape and what organisations across the Life Sciences industry should consider as regulators and sponsors begin preparing for adoption.
19th Jun 2026 13:00 – 14:00 (BST)
Are you ready to transform your skills and unlock your full potential? Now is the time to elevate your training.
Join Now