documents: FDA-2011-N-0915-0004

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0915-0004 FDA FDA-2011-N-0915 Agency Information Collection Activities; Proposed Collection; Submission for Office of Management and Budget Review; Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application Notice 30 Day Proposed Information Collection 2015-06-25T04:00:00Z 2015 6 2015-06-25T04:00:00Z 2015-07-28T03:59:59Z 2015-06-25T13:48:52Z 2015-15638 0 0 0900006481b54bc8

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