Summary of Important 2018 HRPP\IRB Changes

The Human Subjects Office has been working over the last year and a half with the Office of the Vice President for Research and the Human Research Protection Program (HRPP) Taskforce to implement changes based on feedback we have received from the HRPP survey and focus groups.  We are excited to summarize these below changes to the HRPP/IRB review processes to better serve the needs of our research community and the Human Research Protection Program.  

Oct 30 changes

  • Post-approval survey
  • Update to content of the IRB approval memo
  • Elimination of continuing review for qualifying studies


Oct 9 changes

  • Changes to the timing of IRB approval and Pharmacy & Therapeutics Investigational Drug Service approval
  • New Automated UI Health Care Clinical (UIHC) Trials and Research Website recruitment tool


Sept 18 changes

  • HawkIRB Funding Source (Section III) Enhancements


August 2018 changes


Feb 2018 changes