Maptrial eMVR
Centralized Monitoring. Complete Confidence
Maptrial eMVR gives sponsors and monitoring teams real-time, centralized visibility into clinical trial execution across all sites. Monitor data quality, visit progress, queries, SDV, freezes, and locks from a single interface. Automated checks, visual risk indicators, and role-based controls support efficient, compliant risk-based and centralized monitoring, enabling faster issue resolution without slowing down site operations.
Simplify trial management with secure,
accessible clinical data.
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Etiam rhoncus tortor sit amet metus imperdiet, ac hendrerit risus mollis. Nulla facilisi.
Total Visibility. Total Control.
Gain instant, centralized insight into every aspect of study execution. Track data quality, visit progress, queries, SDV, freezes, and locks across all sites in real time. Full audit trails and role-based controls make monitoring efficient, transparent, and fully compliant — giving sponsors and teams complete confidence.
Monitor Smarter. Resolve Faster.
Let Maptrial eMVR handle the heavy lifting. Automated edit checks, high-priority queries, visual cues, and real-time alerts highlight issues proactively. Bulk actions save time, helping monitors resolve problems quickly, keep studies on track, and maintain data integrity with minimal effort and reduced risk.
Built for Modern, Risk-Based Monitoring
Purpose-built for centralized, risk-based trials, Maptrial eMVR combines FDA 21 CFR Part 11–compliant e-signatures, detailed activity logs, and granular permissions. Sponsors gain full traceability, control, and operational efficiency — ensuring studies run smoothly without slowing down site operations.
Learn More About Maptrial eMVR
You Run Trials. Let Us do the Rest.
Find out how the Medigen Suite can fully support your clinical trials, connecting every step of the process and accelerating your path to market.
