dockets: FDA-2000-D-0598

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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-2000-D-0598 FDA Genotoxicity Studies (VICH GL23) Nonrulemaking 2024-11-29T14:40:33Z 0b000064804dd8a9   Guidance finalized 67 FR 602 January 4, 2002; Availability of Revised Guidance 2015     ["VETERINARY MEDICINAL", "DRAFT GUIDANCE", "SAFETY STUDIES", "HUMAN FOOD", "GENOTOXICITY STUDIES", "VETERINARY DRUG RESIDUES", "INDUSTRY", "VICH GL23 R", "TECHNICAL REQUIREMENTS", "APPROVAL", "HARMONISATION", "INTERNATIONAL COOPERATION", "Registration", "2015-308", "open", "#116"] CVM Genotoxicity Studies (VICH GL23)     {"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or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["VETERINARY MEDICINAL", "DRAFT GUIDANCE", "SAFETY STUDIES", "HUMAN FOOD", "GENOTOXICITY STUDIES", "VETERINARY DRUG RESIDUES", "INDUSTRY", "VICH GL23 R", "TECHNICAL REQUIREMENTS", "APPROVAL", "HARMONISATION", "INTERNATIONAL COOPERATION", "Registration", "2015-308", "open", "#116"], "modifyDate": "2024-11-29T14:40:33Z", "dkAbstract": "Guidance finalized 67 FR 602 January 4, 2002; Availability of Revised Guidance 2015", "agencyId": "FDA", "program": "CVM", "shortTitle": "Genotoxicity Studies (VICH GL23)", "subType2": null, "title": "Genotoxicity Studies (VICH GL23)", "generic": "D", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2000D-1631", "subType": null, "category": null, "field2": "OPEN", "effectiveDate": null, "objectId": "0b000064804dd8a9"} single_get

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