Get Access to Expert Insights on ICH GCP E6(R3) Updates
These comprehensive slides, based on a presentation by Sandrine Verstraete, provide a detailed overview of the latest revisions to the ICH GCP E6 (R3) guidelines. With over 25 years of clinical research experience, Sandrine offers a strategic perspective on how these changes impact regulatory compliance, data integrity, and participant protection in clinical trials.
Why You Need These Slides:
- Stay Current with the latest updates from E6 (R2) to E6 (R3).
- Enhance Compliance with insights on updated roles and responsibilities of sponsors, investigators, and ethics committees.
- Quick Reference for professionals involved in clinical trial planning and execution.
Who Should Use These Slides?
Ideal for clinical research associates, project managers, regulatory affairs professionals, and site staff who want to ensure their work aligns with the latest ICH GCP standards.
Key Features:
- Clear, actionable insights
- Focus on real-world applications of E6 (R3)
- Access to a trusted expert’s guidance
Get these slides to stay ahead and refine your approach to clinical research compliance.