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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]
Psychoactive drugs, such as alcohol, caffeine, amphetamine, mescaline, lysergic acid diethylamide (LSD), cannabis, chloral hydrate, theophylline, IBMX and others, have been studied on certain animals. It is believed that plants developed caffeine as a chemical defense against insects.
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.
A generic new animal drug is a copy of an approved new animal drug for which patents or other periods of exclusivity are near expiration. CNADA – A CNADA is used to seek conditional approval of a new animal drug. A conditionally approved CNADA has met all the requirements to support the full approval of the new animal drug except for a ...
Download QR code; Print/export Download as PDF; Printable version; In other projects ... Animal Drug and Animal Generic Drug User Fee Reauthorization Act of 2013;
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.
The FDA animal efficacy rule (also known as animal rule) applies to development and testing of drugs and biologicals to reduce or prevent serious or life-threatening conditions caused by exposure to lethal or permanently disabling toxic agents (chemical, biological, radiological, or nuclear substances), where human efficacy trials are not feasible or ethical. [1]