Welcome, this site enables an Institutional Review Board (IRB) to capture the entire IRB regulatory process, monitor the flow of information and the associated activities and tasks for all participants, delivering a complete electronic document based solution for Human Trials Regulation.
When completing the application, you will be asked to select the review type (exempt, expedited or full board) of the study. Please see http://www.hhs.gov/ohrp/policy/checklists/decisioncharts.html to determine which review type your study qualifies for.
Effective January 1, 2013, the USF Institutional Review Board (IRB) no longer accepts paper submissions for historical "paper" studies. Paper studies that were not converted to the ARC system before this deadline have been administratively closed.