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withdrawn,object_id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-4002-0001,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,2018-11-16T05:00:00Z,2018,11,2018-11-16T05:00:00Z,,2018-11-16T15:25:25Z,2018-25063,0,0,09000064838df0b4