documents: FDA-2009-D-0095-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2009-D-0095-0001 FDA FDA-2009-D-0095 Draft Guidance for Industry on the Clinical Pharmacology Section of Labeling for Human Prescription Drug and Biological Products--Content and Format Notice Notice of Availability 2009-03-03T05:00:00Z 2009 3 2009-03-03T05:00:00Z 2009-06-02T03:59:59Z 2016-11-18T14:37:51Z E9-04372 0 0 09000064808e801c

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