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Guidance Documents/Information-Sheet/Significant Risk and Nonsignificant Risk Medical Device Studies: Guidance For IRBs, Clinical Investigators, and Sponsors

Significant Risk and Nonsignificant Risk Medical Device Studies: Guidance For IRBs, Clinical Investigators, and Sponsors

Detailed guidance document from FDA and regulatory agencies.

Document Details

Information Sheet

January 1, 2006

August 10, 2023

Office of the Commissioner

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