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§ 56.105 Waiver of IRB requirement.

21 CFR 56.105

Citation21 CFR 56.105
CorpusDaily eCFR
Displayed edition2026-09-16
Last updated2026-09-16

§ 56.105 Waiver of IRB requirement.

On the application of a sponsor or sponsor-investigator, the Food and Drug Administration may waive any of the requirements contained in these regulations, including the requirements for IRB review, for specific research activities or for classes of research activities, otherwise covered by these regulations.