Modification Request

A modification request is required if you plan to make any changes to your research or deviate from the protocol after approval or exemption has been granted. Such changes include, but are not limited to:

* Minor changes to the nature of exempt research (such as those with an *) do not require a modification request.

Modification requests should include all the details that would be required for an initial protocol. For example, if making changes to the informed consent process such that subjects will no longer be required to sign a consent form, you must request approval for a waiver of documented informed consent within the modification request. 

Cases in Which New Application May Be Needed

If your planned changes include 1) the addition of a new study population (or group of participants) and 2) changes in procedures (including changes to study instruments), they may not qualify for a modification and you may have to submit a new IRB application. If unsure whether your changes qualify as a modification, contact the HRPP office for guidance. 

Note that changes may not be implemented before your modification request has been approved by the IRB. If you implement changes before IRB approval, you will be out of compliance.

To request a modification of your current approval, complete and submit a Modification Request form to the HRPP office. Remember to submit your request with ample time for the IRB to approve it before you plan to implement the changes.

Note that if your research has been approved as exempt and your modification disqualifies it from its exemption, you must file an initial research protocol with your modification. The modification request and initial research protocol will be reviewed as expedited or by the full committee, as appropriate.