A New Era In Good Clinical Practice Guidelines

The updated ICH GCP E6(R3) guidelines represent a major evolution in global clinical trial conduct — shifting the focus toward patient-centered design, digital enablement, and proactive, risk-based quality oversight. These revisions are reshaping the expectations for how studies are planned, executed, and monitored, signaling a new standard of rigor and flexibility across the research ecosystem.

In this webinar, experts break down the key revisions and explore their implications for all stakeholders, including sponsors, CROs, investigators, and ethics committees. You’ll gain a clear understanding of how these guidelines strengthen data integrity, enhance participant protection, and promote operational efficiency through smarter use of technology and quality-by-design principles.

Watch the presentation to uncover actionable strategies and best practices that will help your organization stay compliant, future-ready, and aligned with the evolving global regulatory framework for clinical research.