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documents: FDA-2011-N-0231-0011

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2011-N-0231-0011 FDA FDA-2011-N-0231 Agency Information Collection Activities: Proposed Collection; Comment Request; Adverse Experience Reporting for Licensed Biological Products; and General Records Notice 60 Day Proposed Information Collection 2020-09-01T04:00:00Z 2020 9 2020-09-01T04:00:00Z 2020-11-03T04:59:59Z 2023-09-07T21:08:45Z 2020-19239 0 0 090000648482d8bb

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