documents: FDA-2014-D-1891-0002

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2014-D-1891-0002 FDA FDA-2014-D-1891 Draft Guidance for Industry on How to Obtain a Letter from FDA Stating that Bioequivalence Study Protocols Contain Safety Protections Comparable to Applicable REMS for RLD Other Guidance 2014-12-05T05:00:00Z 2014 12 2014-12-05T05:00:00Z   2024-11-11T20:55:08Z   1 0 090000648195ee4c

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