Office of the Vice President Research
Human Research Protection Program (HRPP)
The research community at the University of Virginia (UVA) recognizes the immense contribution that human subjects provide the research initiative. The Human Research Protection Program advocates for human subjects in research by working in concert with UVA researchers to ensure that they have the education and tools they need to work ethically with participants in their research studies. UVA’s Institutional Review Board (IRB) & Post-Approval Monitoring (PAM) offices work with the other HRPP partner offices to ensure that compliance with federal regulations and ethical principles create research environments that are proactively protecting participants as researchers achieve their research goals.
The HRPP Staff will be at the 2024 PRIM&R Annual Conference in Seattle from November 17th-20th, 2024. Please be patient with us during this time.
Learn more about the upcoming AAHRPP Reaccreditation Process for UVA's HRPP (behind Netbadge)
Education & TrainingHRPP Standard Operating Procedures Post Approval Monitoring
Huron's IRB System Demonstration video is now available (behind Netbadge)
Please share your thoughts with us as we consider this system while making future plans for UVA's HRPP.
It is the responsibility of each investigator to seek IRB review and approval prior to initiation of any research involving human subjects or before conducting any clinical investigation. However, not all projects are Human Subject Research. To learn more, check out our Non-Human Subject Research page to learn more about these types of project determinations.
UVA is a large institution. To better serve the research community, the university decided years ago to have the IRB specialize by having one side of the IRB focus on serving Biomedical Research (primarily for the health system) and having the other side of the IRB focus on Behavioral Research (primarily for the academic side).
See graphic below. To learn more about which side of the IRB you should submit your study to, please go to our webpage Which side of the IRB should I submit to?
Description of decision process for the specialized sides of the IRB.
Timeline for a Human Subject Research Study
Important Dates
IRB Education & Training
2024 PRIM&R Annual Conference (PRIMR24)
The Seattle Convention Center (SCC) Summit Building in Seattle, WA
2024 PRIM&R Annual Conference (PRIMR24)
The Seattle Convention Center (SCC) Summit Building in Seattle, WA
2024 PRIM&R Annual Conference (PRIMR24)
The Seattle Convention Center (SCC) Summit Building in Seattle, WA
IRB-HSR Full Board Meetings
Virtual
Suggestion Box
Share your thoughts on what you like or any feedback for improvements with us here.
Your ideas will help us to shape future plans for UVA's Human Research Protection Program.
Note, for urgent matters, please see the Compliance Helpline.
IRB review is based on the ethical principles outlined in the Belmont Report, the Nuremburg Code, and the Declaration of Helsinki.
Please refer to our Ethical Principles webpage to learn more.
The University of Virginia's Biomedical and Behavioral Institutional Review Boards (IRB-HSR and IRB-SBS) both apply the federal regulations for the review of human subject research studies as appropriate to the specific research project.
More information can be found on our webpage about the federal regulations.
University of Virginia Institutional Official: Lori McMahon, Vice President for Research
FWA Information
UVA Federal Wide Assurance
FWA#:00006183
Exp. Date: July 7, 2026
More information on UVA's Federal Wide Assurance (FWA) can be found here.
Anonymous Reporting
Allegations of misconduct can be reported confidentially to the University's Research Integrity Officer (RIO) in the Office of the Vice President for Research or through the University's Compliance Helpline.