Regulations.gov document

Informed Consent: Guidance for Institutional Review Boards, Clinical Investigators, and…

Notice · FDA-2006-D-0031 · posted Aug 16, 2023

Key facts

Document ID FDA-2006-D-0031-0138
Title Informed Consent: Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors; Availability
Document type Notice
Subtype Notice of Availability
Agency FDA
Docket FDA-2006-D-0031
Posted Aug 16, 2023
Federal Register citation 88 FR 55703
FR document number 2023-17594
Comment period opens Aug 16, 2023
Effective date Aug 16, 2023

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