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withdrawn,object_id
APHIS-2005-0121-0001,APHIS,APHIS-2005-0121,Draft Guidelines on Pharmacovigilance of Veterinary Medicinal Products: Management of Adverse Event Reports (VICH Topic GL24) and Data Elements for Submission of Adverse Event Reports (VICH Topic GL42),Notice,Availability of a document,2006-01-18T12:15:07Z,2006,1,2006-01-18T12:15:07Z,2006-03-21T04:59:59Z,2008-01-07T22:36:43Z,E6-00445,0,0,0900006480114915
APHIS-2005-0121-0003,APHIS,APHIS-2005-0121,Pharmacovigilance of Veterinary Medicinal Products:  Data Elements for Submission of Adverse Event Reports (VICH Topic GL42),Supporting & Related Material,International standard,2006-01-18T05:00:00Z,2006,1,,,2006-09-02T12:48:25Z,,0,0,09000064800febd4
APHIS-2005-0121-0002,APHIS,APHIS-2005-0121,Pharmacovigilance of Veterinary Medicinal Products:  Management of Adverse Event Reports (VICH Topic GL24),Supporting & Related Material,International standard,2006-01-18T05:00:00Z,2006,1,,,2006-09-02T12:48:24Z,,0,0,09000064800febbf