documents: FDA-2016-D-1280-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-1280-0001 FDA FDA-2016-D-1280 International Conference on Harmonisation: Electronic Transmission of International Conference on Harmonisation; Electronic Transmission of Postmarket Individual Case Safety Reports for Drugs and Biologics, Excluding Vaccines; Availability of FDA Regional Implementation Specifications for ICH E2B(R3) Reporting to the Food and Drug Administration Adverse Event Reporting System Notice Notice of Availability 2016-06-23T04:00:00Z 2016 6 2016-06-23T04:00:00Z   2016-06-23T13:56:49Z 2016-14845 0 0 0900006482060aa9

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