Policies and Guidance Documents
IRB Procedures
- Accessing PHI with Waiver of HIPAA Authorization Updated 11/6/2020
- Adverse Event Procedure Updated 4/1/2019
- Adverse Event Flow Chart Updated 3/28/2019
- Deviation, Violation and Exception Request Procedure Updated 03/05/2020
- Deviation, Violation and Exception Request Flow Chart Updated 03/05/2020
- Frequency of IRB Review and Verification of Material Changes 9/16/2019
- HRPP Written Procedure Revised 7/26/2022
Department Guidance
- Human Research Protection Overview Updated 04/09/2020
- Guidance for IRB Review of QI/QA Projects Updated 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 xForm Updated 01/25/2021
- How to Copy a Submitted xForm 9/10/2021
- Site Permission Letter Template 11/04/2021
- Guidance for QuestionPro RAA 09/10/2024
- Guidance for Human Subjects and Non-Subjects 04/29/2025
- Guidance for Case Reports 01/16/2026
Institutional Policies