ADAMAS Consulting is pleased to announce an exclusive webinar designed to provide critical insights into the newly finalized ICH E6 R3 guidelines. This session, titled “GCP ICH E6 R3 Unveiled: Navigating the Evolving Roles of Sponsors and CROs,” will explore the transformative changes in clinical trial oversight and quality management.
Webinar Details:
- Date: Friday, March 28, 2025
- Time: 10am EDT | 2pm GMT | 3pm CET
- Duration: 60 minutes
On January 6, 2025, a major revision to the ICH E6 guidelines was finalized, marking the beginning of a significant shift in the regulatory landscape. During the implementation phase, regulators will define the mandatory adoption timeline for these changes, making it imperative for industry professionals to understand and adapt to the evolving requirements.
What to Expect:
- In-depth Analysis: Learn about the key structural and content changes introduced in ICH E6 R3 and their impact on clinical trial oversight.
- Evolving Roles: Understand the revised responsibilities of sponsors and Contract Research Organizations (CROs), including shifts in study oversight, risk-based quality management, and overall accountability.
- Strategic Insights: Gain expert perspectives on how to effectively implement updated Good Clinical Practice (GCP) requirements to ensure continuous regulatory compliance and optimize trial efficiency.
Expert Speakers:
With decades of combined regulatory and industry expertise, Dr. Ferrão and Ms. Hutton will share practical strategies and actionable insights tailored for professionals at all levels.
Dr. Elsa Ferrão – GCP Principal Consultant at ADAMAS Consulting
Penelope Hutton – GCP Senior Consultant at ADAMAS Consulting
