Agency for Health Care Policy and Research
Applied Clinical Trials
Belmont Report
Canadian Standards Council
Clinical Trials Networks Best Practices
Department of Health and Human Services
DFR Titles on GPO Access
Ethics - NIEHS Research Ethics
Ethics - Tuskegee University
FDA 21 CFR
FDA (Food and Drug Administration) - Main
FDA CDER (drugs)
FDA CDRH - CFR 21 (Food and Drugs)
FDA Device
FDA Information Sheets
FDA - ORA Compliance Program Guidance 7348.811 (Clinical Investigators)
FDA - ORA Compliance Program Guidance 7348.809 (Institutional Review Boards)
FDA - ORA Compliance Program Guidance 7348.810 (Sponsors, CROs, and Monitors)
FOI - FDA Information and Documentation
Health Canada
ICH - International Conference on Harmonization - Guidelines
National Cancer Institute
NIH - National Institutes of Health
Nuremberg Code
OHRP - Office for Human Research Protection (formerly OPRR)
Regsource.com
Regulatory Affairs Professionals Society
U.S. National Institutes of Health Clinical Trials Registry
U.S. National Library of Medicine (NLM)
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