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withdrawn,object_id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-2015-D-0390-0025,FDA,FDA-2015-D-0390,"Use of Electronic Informed Consent—Questions and Answers; Guidance for Institutional Review Boards, Investigators, and Sponsors; Availability",Notice,Notice of Availability,2016-12-15T05:00:00Z,2016,12,2016-12-15T05:00:00Z,,2016-12-15T15:09:26Z,2016-30146,0,0,090000648240b6b5
FDA-2015-D-0390-0026,FDA,FDA-2015-D-0390,"Use of Electronic Informed Consent Questions and Answers Guidance for Institutional Review Boards, Investigators, and Sponsors",Other,Guidance,2016-12-15T05:00:00Z,2016,12,2016-12-15T05:00:00Z,,2024-11-12T06:17:18Z,,1,0,090000648240bb40