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Application Forms
Determination Form - Complete this form to determine if your research is eligible for IRB exemption or review. Revised 9-2011
To submit a protocol for IRB review, one of the following forms must be submitted. For explanation of exempt, expedited, and full board review, please see the definitions page. Do not submit both forms.
IRB Application (For expedited or full IRB review only) Revised 10-2011
Request for Exemption Application (For exemption only) Revised 8 -2011
Supplement Forms
Below are the supplement forms for use with the IRB Application form. Refer to the form and attach only those that apply to your research protocol.
IRB Supplement Form A - Request for a Waiver of Written Documentation of Consent.
IRB Supplement Form B - Request a Waiver of Consent. Revised
IRB Supplement Form C - Request to use Deception in Research.
IRB Supplement Form D - Use of the Internet in Human Participants Research. Revised 7-2010
IRB Supplement Form E - International Research. Revised 7-2010
IRB Supplement Form F - Research Involving Child Participants.
IRB Supplement Form G - Research Involving Prisoners as Subjects
Other Forms and Documents
Other forms may be required if changes to your protocol occur after IRB approval, or if your research lasts beyond the timeframe of the approval.Modification Request Form – Use to request changes to the originally approved or exempt protocol. Changes in your research protocol cannot be executed without approval.
Add Personnel Form - Use instead of modification request form if the only change to your protocol is new personnel.
Continuation/Termination Request – Use for protocols that have passed their approval date, or to terminate a protocol early. Required to renew approval. Once the timeframe for approval has passed, all research must cease until a new approval or exemption is granted.
Unanticipated Problem Report – Use to report issues that occur within the scope of the research that were not included in the approved or exempt protocol
Informed Consent Checklist – Lists the necessary components of an informed consent document
Informed Consent Template – Use to assist with the drafting of an informed consent form. This template was drafted to assist student researchers.
*Note only the forms contained within these links are considered current. The IRB will not review any previous forms.
