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e-CFR Data is current as of November 19, 2009


Title 21: Food and Drugs
PART 56—INSTITUTIONAL REVIEW BOARDS
Subpart A—General Provisions

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§ 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.

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