documents: FDA-2021-N-0515-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2021-N-0515-0002 FDA FDA-2021-N-0515 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Postmarketing Adverse Experience Reporting and Recordkeeping for Drug and Biological Products Notice 30 Day Proposed Information Collection 2021-11-05T04:00:00Z 2021 11 2021-11-05T04:00:00Z 2021-12-07T04:59:59Z 2021-11-05T17:18:42Z 2021-24236 0 0 0900006484e23a30

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