The Human Research Protection Program (HRPP) reviews and monitors research involving human subjects at UCSF and several affiliate institutions to ensure the welfare, safety, privacy, and ethical treatment of participants in human research studies. Read more about the HRPP program.
The HRPP is comprised of 3 groups:
- Institutional Review Board (IRB), which reviews human subject research studies — learn how to submit to the IRB.
- Quality Improvement Unit (QIU), which conducts monitoring, education and other QI activities.
- Human Gamete, Embryo and Stem Cell Research (GESCR) Committee.
Priority Review for Research on the Health Impact of Changes in Federal Policies since January 2025 and Dobbs Impact Research
The HRPP has appointed a Rapid Review Team (RRT) to ensure Research on the Health Impact of Changes in Federal Policies since January 2025 and Dobbs Initiative Related Research is fast tracked to approval. See instructions on how to request rapid review for studies falling under these categories.
News
- Now in iRIS: New ‘Add Relying Site’ Form + Updated Modification and Application Forms (11/4/24)
- 1 week notice: New 'Adding Relying Site' Form + Updated Modification and Application Forms (10/28/24)
- IRB Limited Meeting Schedule: Impact on Studies Expiring in November, December, January (2024-2025) (10/15/24)
- New Relying Sites Form (10/7/24)
- All News/Bulletins