|
|
|
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 Applcations (INDs)
- 21 CFR Part 812 - Investigational Device Exemptions (IDEs)
- Information Sheet Guidances for IRBs, Investigators and Sponsors
- 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 1200.5 - Requirements for the Protection of Human Subjects in Research
- VHA Forms, Publications & Records Management
[an error occurred while processing this directive]
Last modified: Tuesday, 06-May-2008 20:27:09 PDT