documents: FDA-2016-D-1280-0004

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2016-D-1280-0004 FDA FDA-2016-D-1280 Electronic Submission of Postmarketing Individual Case Safety Reports to the Food and Drug Administration Adverse Event Monitoring System Using International Council of Harmonisation E2B(R3) Data Standards; Regional Data Elements and Implementation Schedule Notice Announcement 2026-04-06T04:00:00Z 2026 4 2026-04-06T04:00:00Z   2026-04-06T21:56:01Z 2026–06660 0 0 09000064b9253a03

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