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FEDERAL REGISTER · NOTICEJune 21, 2024NOTICE — NO LEGAL EFFECT

Human User Safety in New and Abbreviated New Animal Drug Applications; Guidance for Industry; Availability

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Document details are published in the U.S. Federal Register; SPEQ surfaces them for reference and is not affiliated with or endorsed by the FDA or the Office of the Federal Register. The authoritative text is on federalregister.gov.

STATUSNOTICE — NO LEGAL EFFECT
EFFECTIVE—
COMMENTS CLOSE—
APPLIES TO · SPEQ TAGDrugDeviceVeterinary
Document type
Notice
Agency
Health and Human Services Department
Published
June 21, 2024
Document number
2024-13655
Docket
FDA-2023-D-0592
ABSTRACT

The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance for industry (GFI) #278 entitled "Human User Safety in New and Abbreviated New Animal Drug Applications." This guidance is intended for sponsors interested in pursuing the approval, or conditional approval, of new animal drugs (including new generic animal drugs). This guidance addresses general principles of human user safety (HUS) assessment for new animal drugs, sources of data, mitigation strategies for proposed new animal drugs, potential recommendations to address HUS concerns, and how HUS information should be submitted to the Center of Veterinary Medicine (CVM).

Abstract as published in the Federal Register.

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