Implementation Checklist for Centralized Monitoring in Clinical Trials
Centralized monitoring is no longer optional in risk-based monitoring (RBM) frameworks—it is a regulatory expectation and a critical part of modern trial oversight. Yet, successful implementation requires more than installing a dashboard. Sponsors must configure validated systems, define workflows, assign roles, deploy training, and integrate outputs into the Trial Master File (TMF). A checklist-based approach ensures that all components are aligned with GCP requirements and ready for inspection.
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