documents: FDA-2012-D-0847-0002

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id agency_id docket_id title document_type subtype posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2012-D-0847-0002 FDA FDA-2012-D-0847 Draft Guidance for IRBs, Clinical Investigators, and Sponsors; IRB Responsibilities for Reviewing the Qualifications of Investigators, Adequacy of Research Sites, and the Determination of Whether an IND/IDE is Needed Other Guidance 2012-11-20T05:00:00Z 2012 11 2012-11-20T05:00:00Z   2019-10-21T14:42:58Z   0 0 090000648116ec2a

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