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documents: FDA-2003-N-0157-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2003-N-0157-0002 FDA FDA-2003-N-0157 Agency Information Collection Activities; Submission for OMB Review; Comment Request; Guidance for Industry on Submitting and Reviewing Complete Responses to Clinical Holds Notice 30 Day Proposed Information Collection 2003-07-23T04:00:00Z 2003 7 2003-07-23T04:00:00Z 2003-08-23T03:59:59Z 2025-02-27T17:06:53Z 03-18691 0 0 0900006480487912

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