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Instructor:
Sylvain Berthelot, CRScube -
Audience:
Clinical Research Professionals -
Course Duration:
1 hour -
March 11, 2026 at 12:00pm EST
Course overview
This session explores how centralized monitoring and real-time dashboards can be used to proactively identify risk, detect anomalies, and embed quality by design across clinical trials.
This webinar will demonstrate how to interpret visual data for enrollment trends, site performance, and emerging risks, while applying risk-based source data verification strategies and integrated data oversight aligned with ICH guidelines and global regulatory expectations (FDA and EMA).
This webinar will demonstrate how to interpret visual data for enrollment trends, site performance, and emerging risks, while applying risk-based source data verification strategies and integrated data oversight aligned with ICH guidelines and global regulatory expectations (FDA and EMA).