In this free webinar, learn about the most impactful changes in ICH E6 R3 and how they affect trial oversight. The featured speakers will share strategic approaches to implement updated GCP requirements effectively. Attendees will gain insight into ensuring compliance and quality by meeting evolving regulatory expectations. The speakers will also discuss enhancing collaboration between sponsors and CROs under the revised guidelines.
TORONTO, March 10, 2025 /PRNewswire-PRWeb/ -- Discover an informative webinar that will explore the structural and content changes introduced in ICH E6 R3 and their impact on current systems and processes.
On January 6, 2025, a new revision (R3) was finalized and is now in the implementation phase, during which regulators will define its mandatory adoption timeline.
A key focus of this webinar will be the revised roles and responsibilities of clinical research organizations (CROs) and sponsors, including shifts in study oversight, risk-based quality management and accountability. Experts will provide insights on adapting to these changes to ensure continuous compliance and regulatory acceptance while optimizing trial efficiency and integrity.
Register for this webinar to gain expert insights on navigating ICH E6 R3 and staying ahead in clinical trial compliance.
Join experts from ADAMAS Consulting, Dr. Elsa Ferrão (GCP Principal Consultant); and Penelope Hutton, MSc BSc, Cert CRGCP, MRQA (GCP Senior Consultant), for the live webinar on Friday, March 28, 2025, at 10am EDT (3pm CET/EU-Central).
For more information, or to register for this event, visit GCP ICH E6 R3 Unveiled: Navigating the Evolving Roles of Sponsors and CROs.
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