documents: FDA-2025-N-5997-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2025-N-5997-0001 FDA FDA-2025-N-5997 Biosimilar User Fee Act; Stakeholder Consultation Meetings on Biosimilar User Fee Act Reauthorization; Request for Notification of Stakeholder Intention To Participate Notice General Notice 2025-12-12T05:00:00Z 2025 12 2025-12-12T05:00:00Z   2025-12-13T00:47:14Z 2025-22619 0 0 09000064b90c85ad

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