Risk-Based Quality Management (RBQM) for Clinical Trials
Enhance clinical quality oversight and control with a modern risk-based quality management solution built to help sponsors and CROs proactively identify, monitor, and mitigate risks throughout the trial lifecycle.
This RBQM approach empowers teams to shift from reactive issue correction toward data-driven quality assurance. By unifying risk signals from across your trial ecosystem into a consolidated view, you gain earlier insight into emerging risks, stronger centralized monitoring, and better alignment with regulatory expectations.
Cost and efficiency advantage
By centralizing risk oversight and leveraging automated monitoring and alerts, organizations can significantly reduce the time and effort required to detect and address quality issues – often resulting in measurable operational cost savings compared to traditional, manual monitoring approaches, without sacrificing compliance or data quality.
Centralized risk monitoring and analytics
Aggregate diverse data streams into a single, real-time risk dashboard – enabling teams to track trends, detect signals earlier, and prioritize quality interventions.
Configurable risk indicators (KRIs)
Define study-specific risk thresholds and indicators to monitor performance, enrollment, data trends, and protocol compliance with precision.
Automated alerts and escalation workflows
Real-time risk notifications reduce manual review burden while ensuring quality events are surfaced promptly.
Actionable dashboards and reporting
Interactive visualizations, quality reports, and drill-down tools support governance reviews, audit readiness, and cross-functional collaboration.
Integrated with iMednet
Direct integration with the iMednet platform delivers continuous access to the latest clinical data for risk profiling and quality measurement – eliminating redundancy and improving operational agility.
A Complete Solution
Contact us for an introduction to Mednet's comprehensive EDC-centric eClinical platform with key native modules to support all study types and phases – such as randomization, trial supply management, adjudication, ePRO, payments, DICOM imaging, eConsent and more.