Clinical Trial Management System (CTMS)

Clinical Trial Management System

Customized CTMS in a secure web-based, comprehensive clinical trial tracking system. Robust in its capability and very light operating system, viewable in any browser and now with eVisit Reports

We take timelines seriously and work side by side with Sponsors and colleagues to ensure the most efficient path possible while being mindful of duplicated efforts. PRC Clinical utilizes our CTMS to support efficient team communication and assist with planning, managing and reporting overall study timelines.

Real-time study data is available for viewing online via web-based CTMS access and can be granted by role (“Sponsor”, “Project Manager”, “Regional CRA”) to any team member.

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Our CTMS can interface with various EDC and IRT (IWRS randomization) platforms, Central Laboratories, and other study services seamlessly to provide real-time study information and metrics in one, easy to use location. It is 21 CFR Part 11 Compliant.

A powerful and flexible tool for tracking and viewing study information, the PRC Clinical CTMS, tracks and manages all virtually facets of the trial including:

  • Study & site startup activities
  • Electronic and paper Essential Document tracking
  • IRB/EC meeting activity
  • Contracts & budgets
  • Screening and enrollment
  • Study subject activity throughout the trial
  • Regulatory documents (electronic and hard-copy)
  • Monitoring visit reports, calendars and schedules
  • Safety Reporting
  • And much more!

CTMS Reporting and Updates: With more than 25 standard reports available, CTMS data generates routine reports which can be viewed and exported by Sponsors the PRC Clinical team. Many more study specific customized reports can also be created ad-hoc, or as templates to be used throughout the life of the study.