Stay Connected
Join us on Facebook Follow us on linked in Follow us on YouTube
Study Management
CLINTRAK CAPABILITIES


request info

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

GO NOW more

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.