CTMSPrimesoft’s, Clinical Trials Management System (ez-CTMS) is a modular, interoperable and standards-based software application designed to meet needs of a single-site or multi-site global clinical trials of CRO’s or Pharmaceutical clients.

The flexible framework and exceptional breadth of functionality of ez-CTMS benefits the user in creating, planning, managing and monitoring clinical studies along with the budget and finance management.

Our Single Integrated Platform (ez-SourceDocx/ez-EDC/ez-CTMS/ez-DIMS) is Flexible, Scalable and Configurable with unprecedented speed of study deployment.

Integration of the ez-CTMS with our other clinical products like ez-SourceDocx for managing source data at the site, ez-DIMS for randomization and drug/device inventory supply management and ez-EDC for data capture offers the user a comprehensive electronic clinical data management solution for clinical research.

Key Features of CTMS:
  • Study Dashboard : Graphically displays enrollment statistics, study calendar, e-CRF and SAE submissions
  • Study Creation : Create and manage protocols and amendments
  • Study Progress Tracking : Track site and overall aggregate study progress with user-defined indicators
  • Study Monitoring : Build monitor schedules; generate, sign, and submit monitor trip reports electronically
  • Budget and Financials : Build monitoring and site budgets; create payment milestones and manage site/vendor payments
  • Custom Reporting : Use report templates, or let our report builders configure custom reports designed to meet specific business objectives
  • Study Personnel Management : Manage contact data of all personnel associated with your organization, sites and sponsor