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withdrawn,object_id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-1995-D-0288-0030,FDA,FDA-1995-D-0288,"25 Reference 24 - ICH Harmonised Tripartite Guideline The Common Technical Document for the Registration of Pharmaceuticals for Human Use Quality re Chemistry, Manufacturing, and Controls Changes to an Approved Application: Certain Biological Products Draft Guidance for Industry",Supporting & Related Material,Background Material,2018-01-04T05:00:00Z,2018,1,,,2018-01-04T14:41:50Z,,0,0,0900006482d96265
FDA-1995-D-0288-0031,FDA,FDA-1995-D-0288,"26 Reference 25 - ICH Harmonised Tripartite Guideline Validation of Analytical Procedures Text and Methodology re Chemistry, Manufacturing, and Controls Changes to an Approved Application: Certain Biological Products Draft Guidance for Industry",Supporting & Related Material,Background Material,2018-01-04T05:00:00Z,2018,1,,,2018-01-04T14:41:58Z,,0,0,0900006482d962c0