documents: FDA-2012-D-0847-0001

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2012-D-0847-0001 FDA FDA-2012-D-0847 Draft Guidance for IRBs, Clinical Investigators, and Sponsors; Availability: IRB Responsibilities for Reviewing the Qualifications of Investigators, Adequacy of Research Sites, and the Determination of Whether an IND/IDE is Needed Notice Notice of Availability 2012-11-20T05:00:00Z 2012 11 2012-11-20T05:00:00Z 2013-01-23T04:59:59Z 2013-01-25T03:01:05Z 2012-28149 0 0 090000648116eb29

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