Committee on Human Subjects in Research (CHSR)
Links and References
Office for Human Research Protection
- Human Subject Protection – 45CFR46
- International Requirements for Human Subject Protection
- Education
- Frequently Asked Questions
Food and Drug Administration (FDA)
- Food and Drug Administration
- 21CFR 50 (Human Subjects)
- 21CFR 56 (IRB)
- 21 CFR 312 (IND)
- 21CFR 812 (IDE)
- Information Sheet Guidance for IRBs, Clinical Investigators and Sponsors
- A Guide to Informed Consent – Information Sheet