Any study that does not meet the requirements of the other levels of review (non-research, non-human research, exempt or expedited review) must go to full board review in accordance with 45 CFR #46.108, 109 and must meet the standards outlined in 45 CFR #46.111 in order to receive approval from the full board.
Full board review is considered the default type of review. The other classifications and review types (e.g., exempt and expedited) represent special cases with specific parameters that must be met. Having your study called to full board does not automatically mean there are major issues with your protocol. It may only mean the study did not meet the specific criteria for another classification. Protocols in which investigators requested another level of review (e.g., exempt or expedited) may still be routed for full board review if the ORSP Office and/or IRB determines the study does not meet the criteria for that classification.
- Full Board Review Request Form
- Signed Assurance Form – Faculty
- Signed Assurance Form – Student
- Consent Form OR Alteration/Waiver of Consent Form
Also attach, if applicable
- NIH Training Certificates
- Participant solicitations
- Vulnerable Populations Form
- HIPAA/FERPA Form and HIPAA/FERPA Consent Form
The IRB documents have been revised as of January 2018 and can be found in the ORSP Canvas Classroom. You may enroll in the classroom by clicking here.