documents: FDA-2012-D-1168-0002

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2012-D-1168-0002 FDA FDA-2012-D-1168 Draft Guidance for Industry on Providing Submissions in Electronic Format Summary Level Clinical Site Data for CDER's Inspection Planning Other Guidance 2012-12-19T05:00:00Z 2012 12 2012-12-19T05:00:00Z 2013-02-20T04:59:59Z 2013-02-26T03:03:09Z   0 0 090000648119255a

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