A Feature-Rich CTMS
This study-specific web-portal provides the entire team – Sponsors, research sites, and Medpace experts – with a set of collaboration pages for secure posting and sharing of study documents, team-meeting minutes, and other important items and features real-time tracking. ClinTrak® Trial Management System also provides centralized access to prospective Site/Investigator profiles for rapid identification of potential investigators and review of previously conducted feasibility information.
Features:
- Submissions and Site Activations – including country-specific approvals, regulatory document tracking, and Institute Review Board – Ethics Committee (IRB-EC) meeting dates
- Site Personnel and Study Contacts
- Subject Enrollment – including exportable enrollment data available via dashboard graphs and printable reports, as well as direct feeds from ClinTrak® IVRS/IWRS and ClinTrak Lab for a single, accurate source of enrollment metrics
- Electronic Monitoring Trip Reports – automated workflow enters protocol deviations directly into database and allows for rapid turn-around time on report availability
- Site Supply Inventory
