documents: FDA-2001-D-0506-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2001-D-0506-0001 FDA FDA-2001-D-0506 Draft Guidance for Industry on Postmarketing Safety Reporting for Human Drug and Biological Products Including Vaccines; Availability Notice Notice of Availability 2015-03-27T04:00:00Z 2015 3 2001-05-11T04:00:00Z 2001-05-12T03:59:59Z 2015-03-28T02:05:34Z   0 0 09000064804ef987

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