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Regulations and
Regulatory Agencies
- Food and Drug Administration (FDA)
- FDA Informed Consent
- 21 CFR Part 50 - Protection of Human Subjects
- 21 CFR Part 56 - Institutional Review Boards
- 21 CFR Part 312 - Investigational New Drug Applications (INDs)
- 21 CFR Part 812 - Investigational Device Exemptions (IDEs)
- Information Sheet Guidances for IRBs, Investigators and Sponsors
- FDA Frequently Asked Questions
- California Law (Statutes)
- California Protection of Human Subjects in Medical Experimentation Act
- Department of Veterans Affairs (VA)
- Veterans Health Administration (VHA) - Research Programs
- 38 CFR Part 16
- VA Handbook 1200.05 - Requirements for the Protection of Human Subjects in Research
- VHA Forms, Publications & Records Management
Stanford University | Dean of Research | Research Compliance
Human Subjects Federalwide Assurance Number: FWA00000935, 8/14/2001 - 3/5/2012
Medical IRB Nos. 01, 03, 04, 05, 06, 07 & 08 Nonmedical IRB No. 02
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Last modified: Thursday, 17-Sep-2009 16:32:54 PDT