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European Union Clinical Trial Directive (EUCT)
Food and Drug Administration (FDA)Report
National Institutes of Health (NIH)
Office for Human Research Protections (OHRP)
Belmont Report
WMA Declaration of Helsinki
Code of Federal Regulation, CFR Title 21 – Part 50. Protection of Human Subjects
Code of Federal Regulation, FR Title 21 – Part 56. Institutional Review Board
International Conference on Harmonization / Good Clinical Practices (ICH / GCP)
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