documents: FDA-2011-N-0915-0001

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

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2011-N-0915-0001 FDA FDA-2011-N-0915 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products, etc. Notice General Notice 2011-12-27T05:00:00Z 2011 12 2011-12-27T05:00:00Z 2012-02-28T04:59:59Z 2011-12-27T16:45:58Z 2011-33140 0 0 0900006480f89156

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