Policies and Guidance Documents
IRB Procedures
- Accessing PHI with Waiver of HIPAA AuthorizationÌýUpdated 11/6/2020
- Adverse Event ProcedureÌýÌýUpdated 4/1/2019
- Adverse Event Flow ChartÌýUpdated 3/28/2019
- Deviation, Violation and Exception Request ProcedureÌýUpdated 03/05/2020
- Deviation, Violation and Exception Request Flow ChartÌýUpdated 03/05/2020
- Frequency of IRB Review and Verification of Material ChangesÌý New 9/16/2019
- HRPP Written Procedure Revised 7/26/2022
Department Guidance
- Human Research Protection OverviewÌýUpdated 04/09/2020
- Guidance for IRB Review of QI/QA ProjectsÌýUpdated 08/13/2020
- Guidance for Obtaining Informed Consent via Telephone Updated 12/15/2020
- Guidance for Online Tools for Research Activities, Data Collection and Storage Updated 08/20/2024
- What Reviewers Need From Your Research Application
- Guidance for Removal of Individual Identifiers from information/Records/Samples
- Guidance for Research Involving Children
- Guidance for Student Researchers
- Guidance for When to Submit an FYI xFormÌýUpdated 01/25/2021
- How to Copy a Submitted xForm New 9/10/2021
- Site Permission Letter Template New 11/04/2021
Institutional Policies
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