Forms and Templates
IRB Expedited or Full Board Review
Initial Review documents (required):
- F-01 Initial Application
- T-01 IRB protocol template
(Note: the use of this template(T-01) is encouraged but not required. If you are required to use another type of protocol template by a sponsor or collaborating institution, please submit a protocol in that required template. You should only have one protocol document.)
Consent documents (as required based on your submission):
Additional documents (as required based on your submission):
- F-02 Supplement, Vulnerable Populations
- F-03 Supplement, International Research
- F-04 Supplement, Drugs, Biologics, Supplements and Botanicals
- F-05 Supplement, Devices
- F-06 Supplement, Dept of Defense
- F-07 Request for Waiver or Alteration of Consent
- F-08 Request for Waiver of Documentation Of Consent
All other forms:
- F-09 Continuing Review
- F-11 Change to Research Protocol
- F-12 Research Closure Form
- F-13 Response to Required Modifications
- F-14 Reportable Information Form
- F-17 Change to Research Personnel
- F-18 Request of Waiver of Alteration of Consent for Public Benefit and Service Program
- F-19 Annual Status Report
Exempt review
Initial Review documents (required):
Consent documents (as required based on your submission):
- T-06 Exempt Consent Form Template with guidance
- T-07 Exempt Consent Template without guidance
- If substantive changes are made to previously exempted research, submit F-11 Change to Research Protocol for a re-determination of exemption status.
Non-Human Subject Research (non-HSR) Determination
If you would like a formal determination of non-HSR status, submit F-16 Determination of Human Subjects Review Form.
