documents: FDA-2018-N-4002-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2018-N-4002-0002 FDA FDA-2018-N-4002 Electronic Submission of Adverse Event Reports to the Food and Drug Administration Adverse Event Reporting System Using International Council for Harmonisation E2B(R3) Standards; Public Meetings; Request for Comments Notice Request for Comments 2019-03-14T04:00:00Z 2019 3 2019-03-14T04:00:00Z 2019-04-26T03:59:59Z 2024-11-12T22:56:38Z 2019-04730 1 0 0900006483ade980

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