Category:Regulation USA
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Clinical research regulation in the United States
This category explains the main U.S. regulations and requirements that govern clinical research. It describes how clinical trials are approved, conducted, and overseen, and how the rights and safety of human subjects are protected.
The category covers key federal regulations such as 21 CFR 312 and 45 CFR 46, as well as related topics including institutional review boards, sponsor-investigators, and the overall U.S. clinical research regulatory framework.
Pages in category "Regulation USA"
The following 5 pages are in this category, out of 5 total.