The AIDS reader
IRB/FDA requirements relevant to HIV/AIDS clinical trials in correctional settings
Abstract
Federally funded research involving inmates in US correctional facilities requires the approval of the Office for Protection from Research Risks (now called the Office for Human Research Protections [OHRP] and located in the Office of the Secretary of the Department of Health and Human Services). Trials that are carried out by pharmaceutical companies (not federally funded) fall under the jurisdiction of the FDA. This article reviews OHRP and FDA guidelines relevant to the conduct of HIV/AIDS clinical trials in correctional settings.
Source and rights
Published by The AIDS reader, 2001. The guideline itself is at the source linked here.
Prognia summarises this guideline for reference and education. It is not medical advice. Always check the official guideline and current local protocols before acting on it.
At a glance
- Published
- 2001
- Applies to
- 🇺🇸 United States
- Scope
- National
- Journal
- The AIDS reader
- PubMed
- 11215087
- Added to Prognia
- 25 July 2026




