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documents: FDA-2015-D-0390-0025

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2015-D-0390-0025 FDA FDA-2015-D-0390 Use of Electronic Informed Consent—Questions and Answers; Guidance for Institutional Review Boards, Investigators, and Sponsors; Availability Notice Notice of Availability 2016-12-15T05:00:00Z 2016 12 2016-12-15T05:00:00Z   2016-12-15T15:09:26Z 2016-30146 0 0 090000648240b6b5

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