documents: FDA-2011-D-0597-0050

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2011-D-0597-0050 FDA FDA-2011-D-0597 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Draft Guidance for Industry; Oversight of Clinical Investigations; A Risk-Based Approach to Monitoring Notice 30 Day Proposed Information Collection 2012-09-25T04:00:00Z 2012 9 2012-09-25T04:00:00Z 2012-10-26T03:59:59Z 2015-07-07T16:54:15Z 2012-23545 0 0 090000648112654c

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