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


Contact the IRB staff

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