The Indiana University Human Research Protection Program (HRPP) provides administrative support to all IU campuses and maintains physical offices in two locations, Indianapolis and Bloomington.
If your research involves human subjects or is regulated by the Food and Drug Administration (FDA), it requires review and approval from an institutional review board (IRB) or the Human Subjects Office.
Start by answering these questions:
If you answered yes to either of the above, then your study requires human subjects review and approval. This may mean obtaining review and approval from an institutional review board or confirmation that your human subjects research is exempt from IRB review.
After submission, a professional staff member in the Human Subjects Office will pre-review your submission and any attached documents. If the staff member, or screener, has any questions or requests for revisions, the submission will be returned to you with those comments. Your submission will not be processed until you have addressed the screener’s comments and re-submitted your study. If you do not respond within two weeks, your submission may be withdrawn.
Once your study is approved, you will receive notifications via email, prompting you to visit Kuali Protocols to retrieve your approval documents, which you will need to keep for your records.
For more information, visit: https://research.iu.edu/compliance/human-subjects/index.html