ClinOps VPs, study managers, and CRA managers are often frustrated by missing data and error-prone manual workflows. Comprehend solves these problems by automating oversight and collaboration across studies, systems, and CROs at every stage.
Track the status of each study in real time and proactively identify issues that could cause milestone delays.
- Integrate data from your CTMS, EDC, ePRO, IxRS, and other data systems and automate updates
- Quickly identify and address issues to optimize study start-up, enrollment, and compliance
- Gain actionable insights about the productivity of sites, countries, and CRAs
CRO Oversight & Collaboration (a ClinOps Insights add-on)
ClinOps VPs, study managers, and vendor managers use this solution to make the most of their CRO relationships. Reduce cycle times and improve data quality by monitoring CRO quality agreements and oversight plans in real time.
- Automate KPIs and thresholds to ensure quality and compliance with regulations such as ICH E6(R2)
- Use real-time performance dashboards to quickly monitor each CRO, study, site, and KPI
- Resolve issues quickly through collaborative task management
Comprehend’s Centralized Monitoring solution enables ClinOps professionals to go beyond traditional site operations. A risk-based management (RBM) approach lowers costs and saves time by helping you think more strategically about site visits.
- Reduce compliance and regulatory risk through early notification of data issues
- Allocate site visitation resources more effectively
- Use custom KRIs and root-cause analysis to identify and address issues more quickly
KPI Studio gives ClinOps professionals an easy way to create user-defined reports and visualizations, based on the data points that are most meaningful to each stakeholder.
- Access raw data from all your systems—EDC, CTMS, etc.—and create your desired KPIs and analytics
- Enjoy drag-and-drop functionality with no coding required
- Easily generate tabular and visual reports for presentations and internal review
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Let us help you overcome your clinical trial challenges.