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Study Management
CLINTRAK CAPABILITIES


Medpace ClinTrak EDC Demonstration

Medpace ClinTrak IWRS-EDC Demonstration


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Medpace is ready to help you with your next clinical trial project. Find out more about how we can help.

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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.