documents: FDA-2008-D-0576-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2008-D-0576-0002 FDA FDA-2008-D-0576 Guidance for Sponsors, Clinical Investigators, and IRBs - Data Retention When Subjects Withdraw from FDA-Regulated Clinical Trials Other Guidance 2008-10-01T04:00:00Z 2008 10 2008-10-01T04:00:00Z   2024-11-07T22:00:24Z   1 0 09000064807c73e0

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