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withdrawn,object_id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-4002-0007,FDA,FDA-2018-N-4002,"Electronic Submission of Adverse Event Reports to the Food and Drug Administration Adverse Event
Reporting System Using International Council of Harmonisation E2B(R3) Standards; Public Meeting; Request for Comments",Notice,Public Meetings,2023-02-17T05:00:00Z,2023,2,2023-02-17T05:00:00Z,2023-12-07T04:59:59Z,2023-12-07T02:04:00Z,2023-03372,0,0,09000064856b6f60