Managing Protocol Deviation In Clinical Research
This webinar brings together clinical research professionals working across site, operations, and quality roles to share practical, real-world insights into how protocol deviations are managed in clinical trials.
The speakers will walk through how these issues arise during study conduct, how they are handled across different levels, and how they impact overall trial outcomes.
During this session, we will cover:
How protocol deviations occur in real clinical trial settings.
The impact of deviations on data quality, timelines, and study outcomes.
How deviations are identified, documented, and managed across teams.
The role of site, operations, and quality in handling protocol deviations.
What regulators and auditors look for during review and inspection.
Common gaps, root causes, and practical approaches to prevention.
This session is ideal for clinical research professionals across sites, CROs, and sponsor teams — including investigators, CRAs, study coordinators, project managers, and quality or regulatory professionals involved in the conduct and oversight of clinical trials.
📅 Friday, May 29, 2026
⏰ 4:00 PM WAT
📍 Virtual (Open to participants globally)