The program will assist investigators to learrn:

  • The ethical, scientific and legal reasons for clinical trials registration and reporting
  • Which trials are required to be registered and the timelines
  • Tips, tricks and helpful content to improve the process
  • The regulations and current performance gaps
  • Resources and assistance available

To view a recent information session discussing the program, download the attached pdf Powerpoint, the one-page handout or view the video.


Click the pages below to learn more:

  • Timeline
  • Program Highlights
  • Registering and Reporting
  • Trials to Register and Report
  • Responsible Party
  • Registration Information
  • Updating a Study in-Process
  • Submitting Basic Results
  • Helpful Links
  • Common Errors
  • Legacy and Terminated Studies
  • Selected Publications