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Guidance Documents/Guidance-Document/Exception from Informed Consent Requirements for Emergency Research: Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors

Exception from Informed Consent Requirements for Emergency Research: Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

April 1, 2013

February 3, 2025

Office of the Commissioner

c1c4c389-82e0-4459-b587-78c877667c9b

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