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dockets: FDA-2025-P-1807

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

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id agency_id title docket_type last_modified object_id rin dkabstract category subtype keywords program short_title effective_date organization attrs_raw attr_source
FDA-2025-P-1807 FDA Petition for Reclassification of Covid-19 mRNA And Adenoviral Vector Products as Gene Therapy Products and for Regulatory Action Regarding the Statutory Violations and International Legal Contraventions Inherent in the Covid-19 Countermeasures Program Nonrulemaking 2026-09-30T18:49:09Z 0b000064b8e1d8d9                     list_pull

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