US Department of Health and Human Services (HHS) Regulations for the Protection of Human Subjects (CFR 45 Part 46)
- : Implements the basic ethical principles governing the conduct of human subjects research as outlined in the "Belmont Report".
US Food and Drug Administration (FDA) Regulations (21 CFR Part 56 - IRBs and 21 CFR Part 50 – Informed Consent)
- : Regulations that govern human subjects research relating to clinical investigations of FDA regulated products (i.e., drugs, devices, or biologics).
- : Information on HIPAA specific to use of patient data in research.