Clinical Trial Management System
Critical support to ensure success and efficient delivery at every phase of global trials
Critical support to ensure success and efficient delivery at every phase of global trials
A Feature-Rich Clinical Trial Management System (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.
Our Proprietary ClinTrak® CTMS Features:
- Submissions and Site Activations – including country-specific approvals, regulatory document tracking, and Institutional 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
ClinTrak Demo
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