CTMS
Clinical Trial Management System
Our CTMS provides a single, centralized platform to orchestrate operational and administrative activities for clinical studies. It features easy setup for study startup, site/user management, screening criteria (inclusion and exclusion), visit alerts, milestone alerts, email delivery system, monitoring plans matrix reports, etc.
Study Startup:
- Investigator, site selection and management
- Investigator and site assessments
- User role management and access control
Study Management
- Milestone and recruitment tracking
- Email notification for any study related events
- Drug shipment tracking and supplies management
- Subject, visit, CRFs and query tracking
- Monitoring visit plan, SDV tracking and reports
- Subject exemptions and deviations tracking
- SAE tracking alerts and notifications, including CIO reporting
- Study documents management
- Study progress tracking and Status reports
