21 CFR 56.105 - Waiver of IRB requirement.
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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.
Title 21 published on 2014-04-01.
No entries appear in the Federal Register after this date, for 21 CFR Part 56.