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Animal Drugs The Federal Food, Drug, and Cosmetic Act gives FDA the legal authority to approve and regulate drugs for animals. Before a drug company can market an animal drug, the company must get the drug approved by FDA.
Animal handling and restraint hazards Most bite, scratch, kick, and crush injuries from animals can be prevented by using appropriate restraint and following established procedures. docHub injuries and medical emergencies may result if proper procedures are not followed or precautions are not taken.
Animal Medicinal Drug Use Clarification Act (AMDUCA) of 1994. 21 CFR 530.41 - Drugs prohibited for extralabel use in animals.
As mandated by the Federal Food, Drug, and Cosmetic Act (the act), a new animal drug may not be sold into interstate commerce unless it is the subject of an approved new animal drug application (NADA), abbreviated NADA (ANADA), or there is a conditional approval (CNADA) in effect pursuant to 21 U.S.C.
(The target animal species is the specific animal species that the drug will be used in.)
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These tests are conducted to evaluate drug safety in two different animal species, with animals receiving high doses of the new drug for 30 or 90 days. Animals are carefully monitored for side effects. After the study period, pathologists examine their organs for signs of drug toxicity.

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