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The requirement for a VFD was created by the Animal Drug Availability Act 1996 (P.L. 104-250). [1] Regulations related to the VFD are published by the FDA's Center for Veterinary Medicine in 21 CFR 510, 514, and 558. [1] A VFD is required for any species of animal fed medicated feed containing a VFD drug; this law is not limited to livestock. [2]
A “Type C medicated feed” is intended as the complete feed for the animal or may be fed “top dressed” (added on top of usual ration) on or offered “free-choice” (e.g., supplement) in conjunction with other animal feed. It contains a substantial quantity of nutrients including vitamins, minerals, and/or other nutritional ingredients...
The animal feed sector is valued at $400 billion in 2018 and is forecasted to grow by $92 billion in 2020 to 2024 with a compound annual growth rate (CAGR) of 4% based on the animal feed market ...
The Animal Drug Availability Act 1996 (ADAA) is a United States federal law. President Clinton signed the ADAA into law in October 1996. While still obligated to public health concerns, the Act intends more rapid drug approval and medicated feed approval to assist the animal health industry.
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The American Feed Industry Association (AFIA) is a not-for-profit organization that represents the feed industry in industry-wide events, national and state legislation, etc. Members of the AFIA include livestock feed manufacturers, ingredient suppliers, pet food manufacturers, supplier companies, regional and state associations, and international firms.
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