• Use for stand-alone study creation, or integrate seamlessly with iRIS review board modules to complete the entire study application process, from creation to approval
  • Get relief from arduous administrative tasks by eliminating stacks of paper
  • Communicate easily via internal messaging and notifications as well as coordinated external emails


  • Let CTMS Software help you organize the process of clinical trial creation and submission
  • Track researcher training, manage milestones, subjects, and integrated budgets, and coordinate meetings— all within the same software


  • Build and manage clinical trial study arms, visits, cycles, and procedures
  • Review and audit institutional regulations and compliance
  • Utilize powerful scheduling component of CTMS software to set meeting dates and times, manage your appointment calendar, and oversee personnel and resource scheduling
Ideal for clinical researchers and research administrators at public and private hospitals and universities, iRIS CTMS software has everything you need to organize your clinical trials. Guide the study process effectively and efficiently while complying with all necessary regulations.