documents: FDA-2009-N-0592-0089

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2009-N-0592-0089 FDA FDA-2009-N-0592 Reference 15 - "Guidance for Sponsors, Institutional Review Boards, Clinical Investigators and FDA Staff: Guidance on Informed Consent for In Vitro Diagnostic Device Studies Using Leftover Human Specimens That Are Not Individually Identifiable, April 25, 2006" - [Informed Consent Elements; Final Rule] Supporting & Related Material BKG-Background Material 2011-01-04T05:00:00Z 2011 1     2011-06-11T16:28:11Z   0 0 0900006480bc3e0f

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