Regulations
- Code of Federal Regulations
- Food & Drug Administration (FDA)
- Information for Health Professionals
- Center for Devices and Radiological Health
- FDA 21 CFR 50—Protection of Human Subjects
- FDA 21 CFR 56—Institutional Review Boards
- FDA 21 CFR 312—Investigational New Drugs
- FDA 21 CFR 812—Investigational Device Exemptions
- Department of Health and Human Services, Office of Human Research Protections (OHRP)
- National Institutes of Health (NIH)
- Office of Human Subjects Research
- National Human Genome Research Institute Policy & Ethics
- Computer-Based Training for Human Subjects Researchers
- NIH 45 CFR 46—Protection of Human Subjects
- Minors as Research Subjects
- DOE—Protecting Human Subjects Home Page
