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withdrawn,object_id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-2008-D-0576-0001,FDA,FDA-2008-D-0576,"Guidance for Sponsors, Clinical Investigators, and IRBs; Data Retention When Subjects Withdraw From FDA-Regulated Clinical Trials; Availability",Notice,NAD-Notice of Availability of Data,2008-12-01T05:00:00Z,2008,12,2008-12-01T05:00:00Z,,2024-11-12T04:25:37Z,E8-28387,1,0,09000064807c7038
FDA-2008-D-0576-0002,FDA,FDA-2008-D-0576,"Guidance for Sponsors, Clinical Investigators, and IRBs - Data Retention When Subjects Withdraw from FDA-Regulated Clinical Trials",Other,Guidance,2008-10-01T04:00:00Z,2008,10,2008-10-01T04:00:00Z,,2024-11-07T22:00:24Z,,1,0,09000064807c73e0