The following forms and templates should be used to submit your research to the IRB. (ADA Compliant Forms are available at the bottom of the page.)

Note: Always check here to ensure you are using the most current version of each form and/or template. 

Note, all of the following forms are available from within the corresponding submission in eRA.

  • HRP-213: FORM - Amendment—This form is a required attachment for all amendment submissions.
  • HRP-214: FORM - New Information—This form is a required attachment for a new information submission such as an unanticipated problem or adverse event. See page 2 of the form for more specific examples. 
  • The Continuing Review and Final Review now use an e-Form, similar to the Initial Application Form.  Do not submit the old HRP-212 Continiuing/Final Review Form in these submission types.

The following template provides essential topics of interest that the IRB looks for during review. Use the template to build your initial protocol document.  Remove all template guidance before you attach the file to the submission. The template guidance is only intended to help you draft the document and should not be retained in the final version.

Use the Consent Document template to draft the consent form(s) for your study.  This template includes extensive guidance that you should consider.  Remove all template guidance before you attach the file to the submission. The template guidance is only intended to help you draft the document and should not be retained in the final version.

Use the Pre-screening Consent Script template to describe activities being done before obtaining informed consent.

The following template provides guidance for investigators who will conduct research outside of the United States. Use the template to build a Local Review Letter.

The following documents are ADA compliant versions of the HRP submission forms, consent document, and protocol template.