A feature-rich and fully customizable Clinical Trial Management System (CTMS) that utilizes multiple data streams to record trial patient data. 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 of:
- 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 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 also provides centralized access to Prospective Site/Investigator Profiles for rapid identification of potential investigators and review of previously conducted feasibility information.