§ 56.105. Waiver of IRB requirement.
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/us/cfr/t21/s§ 56.105·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
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.
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§ 56.105
Waiver of IRB requirement.
Fed. Reg.×2
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