🐄New Import Regulations to Combat Foot-and-Mouth Disease
The Department of Agriculture has proposed a certification requirement for importing farm equipment to prevent the spread of foot-and-mouth disease. Exporters must provide proof of proper cleaning prior to export, affecting compliance processes and restrictions for impacted businesses. Comments on the information collection request are open until March 2025.
Learn More🐴USDA's Equine 2026 Study
In accordance with the Paperwork Reduction Act of 1995, this notice announces the Animal and Plant Health Inspection Service's intention to request the reinstatement of an information collection to conduct the National Animal Health Monitoring System's Equine 2026 Study.
Learn More🚫Nicaragua Added to Screwworm List
We are advising the public that we have added Nicaragua to the Animal and Plant Health Inspection Service (APHIS) list maintained on the APHIS website of regions considered affected with screwworm. We took this action because of the confirmation of screwworm in this region.
Learn More🐄New Import Regulations for Animals from Panama and Costa Rica
We are advising the public that we have added Panama and Costa Rica to the Animal and Plant Health Inspection Service (APHIS) list maintained on the APHIS website of regions considered affected with screwworm. We took this action because of the confirmation of screwworm in these regions.
Learn More🚫Guatemala and Honduras Added to Screwworm Regulation List
We are advising the public that we have added Guatemala and Honduras to the Animal and Plant Health Inspection Service (APHIS) list maintained on the APHIS website of regions considered affected with screwworm. We took this action because of the confirmation of screwworm in these regions.
Learn More🐾FDA Seeks Input on Cannabis-Derived Products in Veterinary Use
The Food and Drug Administration (FDA, the Agency, or we) is soliciting comments from the public, particularly veterinarians, related to the use of cannabis-derived products (CDPs) in animals, with an emphasis on cannabidiol (CBD) products and general trends associated with those products, including information about: usage trends (e.g., product selection, indications, etc.), quality standards, benefits of use, potential drug interactions, adverse events and safety problems, and toxicological concerns. This information will enhance the Center for Veterinary Medicine's (CVM's) knowledge of potential safety signals associated with these products, in addition to aiding our understanding of veterinarians' experiences related to the use of CDPs for their animal patients.
Learn More🐾FDA Guidance on Type VII Veterinary Master Files for R&D Released
The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a draft guidance for industry (GFI) #260 entitled "Type VII Veterinary Master File for Research and Development and Risk Reviews." This draft guidance, when finalized, will describe FDA's current thinking regarding the use of Type VII Veterinary Master Files (Type VII VMFs). Type VII VMFs are appropriate for research and development of animal cells, tissues, and cell- and tissue-based products (ACTPs), gene therapies, and heritable intentional genomic alterations (IGAs) in animals.
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