Minimal Risk Studies
The IRB reviews minimal risk studies under the expedited review process on a day-to-day basis. Complete the applicable forms below.
Key facts
Expedited review
Reviewed on a day-to-day basis rather than waiting for a monthly Board meeting.
Minimal risk
For studies determined to be no greater than minimal risk to participants.
Submit via IRBNet
All submissions go through IRBNet for review and documentation.
Minimal Risk forms
Complete the applicable forms below and submit through IRBNet.
Form names are placeholders, to be provided by the IRB Team.
Informed consent video
A short video on the informed consent process to support your submission.
Watching this short overview can help you prepare consent materials that meet IRB expectations for minimal risk studies.
Post-approval submissions
For post-approval issues such as amendments, continuing reviews, reportable events, or closures, more information is included with this submission type. [Post-approval links to be provided by the IRB Team.]
Not sure this is the right submission type?
Contact the IRB Team before submitting through IRBNet.