documents: FDA-2011-N-0915-0003

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0915-0003 FDA FDA-2011-N-0915 Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application Notice 60 Day Proposed Information Collection 2015-01-23T05:00:00Z 2015 1 2015-01-23T05:00:00Z 2015-03-25T03:59:59Z 2015-03-24T02:04:49Z 2015-01111 0 0 09000064819db747

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