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The U.S. Food and Drug Administration (FDA) has the broad mandate under the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321 et seq.) to assure the safety and effectiveness of animal drugs and their use in all animals, including farm animals. The division of the FDA responsible for this is the Center for Veterinary Medicine (CVM). [1]
A new animal drug is defined, in part, as any drug intended for use in animals other than man, including any drug intended for use in animal feed but not including the animal feed, the composition of which is such that the drug is not generally recognized as safe and effective for the use under the conditions prescribed, recommended, or ...
Bottlenose dolphins were administered LSD in the 1960s as part of NASA-funded experiments by John C. Lilly to study human–animal communication. The drug caused the animals to become more vocal, but did not enable meaningful communication. [30] [31] [32]
Drug use in animals may refer to: Animal drug, pharmaceuticals intended for use in animals, especially livestock; Effect of psychoactive drugs on animals, as a result of research studies; Recreational drug use in animals, a behavior in which animals seek out intoxicants for their pleasurable effects; Zoopharmacognosy, a behavior in which ...
Minor animal species include animals other than cattle, swine, chickens, turkeys, horses, dogs, and cats. CVM monitors the safety of animal foods and medications. Much of the center's work focuses on animal medications used in food animals to ensure that significant drug residues are not present in the meat or other products from these animals.
English. Read; Edit; View history; Tools. ... Animal drug; Animal Drug and Animal Generic Drug User Fee Reauthorization Act of 2013 ... Wikipedia® is a registered ...
A separate issue is the use of testing on animals as a means of initial testing during drug development, or actual production. [40] Guiding principles for more ethical use of animals in testing are the Three Rs first described by Russell and Burch in 1959. [41] These principles are now followed in many testing establishments worldwide.
This article incorporates public domain material from websites or documents of the Congressional Budget Office. [1]The Animal Drug and Animal Generic Drug User Fee Reauthorization Act of 2013 would authorize the collection and spending of fees by the Food and Drug Administration (FDA) for certain activities to expedite the development and marketing approval of drugs for use in animals.