documents: FDA-2016-D-1280-0005
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-1280-0005 | 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 | 2026-04-06 | 2026 | 4 | 2026-04-06 | 2026-10-02 | 2026-04-07 09:00:25 | 2026-06660 | 1 | 0 | 09000064b9253dbc |