dockets: FDA-2003-N-0385

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

Data license: Public Domain (U.S. Government data) · Data source: U.S. government sources, plus a few identifier registries; each is listed on the methodology page

This data as json

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-2003-N-0385 FDA Draft Animal Cloning Risk Assessment re FDA-2008-N-0033 Nonrulemaking 2021-09-01T01:03:12Z 0b0000648049a3f0   Q: Why is Docket now FDA-2008-N-0033? A: On January 16, 2008, when the FR Notice published announcing the Draft Risk Assessment the legacy Docket (2003N-0573) was pending migration into the Federal Dockets Management System (FDMS); hence, a new docket had to be created for the FR document     ["guidance", "RISK ASSESSMENT", "Cloning", "Animal ", "2008-N-0033"] CVM Draft Animal Cloning Risk Assessment     {"displayProperties": [{"name": "abstract", "label": "General Information", "tooltip": "Describes an agency's specific regulatory action; equivalents: Abstract, Description, Docket Subject, Related To, Summary."}, {"name": "legacyId", "label": "Legacy ID", "tooltip": "A pre-FDMS agency specific identifier migrated from a legacy system."}, {"name": "generic", "label": "Docket Item Code", "tooltip": "An agency specific code that identifies the type of document that established the docket (regulatory action)."}, {"name": "program", "label": "Center", "tooltip": "The agency specific program associated with the docket (regulatory action); equivalents: Docket Item Code, Location."}, {"name": "field2", "label": "Docket Status", "tooltip": "Used to Identity that a Docket's Status is Open or Closed"}, {"name": "shortTitle", "label": "Short Title", "tooltip": "A combination of letters and or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["guidance", "RISK ASSESSMENT", "Cloning", "Animal ", "2008-N-0033"], "modifyDate": "2021-09-01T01:03:12Z", "dkAbstract": "Q: Why is Docket now FDA-2008-N-0033?\nA: On January 16, 2008, when the FR Notice published announcing the Draft Risk Assessment the legacy Docket (2003N-0573) was pending migration into the Federal Dockets Management System (FDMS); hence, a new docket had to be created for the FR document", "agencyId": "FDA", "program": "CVM", "shortTitle": "Draft Animal Cloning Risk Assessment", "subType2": null, "title": "Draft Animal Cloning Risk Assessment re FDA-2008-N-0033", "generic": "N", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2003N-0573", "subType": null, "category": null, "field2": "CLOSED", "effectiveDate": null, "objectId": "0b0000648049a3f0"} single_get

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