For Researchers
Submitting to the IRB
Individuals permitted to serve as PI of human subject research
Electronic submission system for new studies, modifications, continuing reviews, and reportable new information
Find required templates and other forms for submitting to the IRB
Instructions and guidance for the IRB application process
IRB meeting dates, submission deadlines, and review fees
Guidance for multi-site research involving reliance on a single IRB (sIRB)
IRB Policies & Guidance
Current IRB policies and procedures guiding the conduct of human subjects research
Guidance from the IRB on special topics
Information about regulatory changes effective January 21, 2019
Information about registering clinical trials and reporting results
Training & Disclosure Requirements
Training requirements for all researchers involved in human subjects research
Training requirements for researchers conducting NIH-supported clinical trial research
Financial interest disclosure requirements for all covered individuals
Contacts
Contact the IRB staff
Tell us about your recent experience