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- 21 CFR 50 is a regulation that applies to all clinical investigations regulated by the Food and Drug Administration (FDA). It covers clinical investigations supporting applications for research or marketing permits for various FDA-regulated products, including drugs, medical devices, biological products, and electronic products1. The regulation allows exceptions from the general requirements for informed consent in specific situations, such as life-threatening emergencies2.Learn more:âś•This summary was generated using AI based on multiple online sources. To view the original source information, use the "Learn more" links.
(a) This part applies to all clinical investigations regulated by the Food and Drug Administration under sections 505 (i) and 520 (g) of the Federal Food, Drug, and Cosmetic Act, as well as clinical investigations that support applications for research or marketing permits for products regulated by the Food and Drug Administration, including foods, including dietary supplements, that bear a nutrient content claim or a health...
www.ecfr.gov/current/title-21/chapter-I/subchapter-…Currently, FDA’s regulations governing the protection of human participants (21 CFR parts 50 and 56) allow exception from the general requirements for informed consent only in life-threatening situations when certain conditions are met (21 CFR 50.23) or when the requirements for emergency research are met (21 CFR 50.24).www.unr.edu/research-integrity/human-research/h… - People also ask
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