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Forms and Templates

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):

All other forms:

Initial Review documents (required):

Consent documents (as required based on your submission):

If substantive changes are made to previously exempted research, submit F-11 Change to Research Protocol for a re-determination of exemption status.

If you would like a formal determination of non-HSR status, submit F-16 Determination of Human Subjects Review Form.