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Animal Drug Availability Act 1996
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Animal Drug Availability Act 1996 : ウィキペディア英語版
Animal Drug Availability Act 1996

| leghisturl = http://thomas.loc.gov/cgi-bin/bdquery/z?d104:HR02508:@@@R
| introducedin = House
| introducedbill =
| introducedby = Wayne Allard (RCO)
| introduceddate = October 19, 1995
| committees = House Commerce
| passedbody1 = House
| passeddate1 = September 24, 1996
| passedvote1 = agreed voice vote
| passedbody2 = Senate
| passedas2 =
| passeddate2 = September 25, 1996
| passedvote2 = passed unanimous consent
| conferencedate =
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| signedpresident = William J. Clinton
| signeddate = October 9, 1996
| unsignedpresident =
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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 and medicated feed approval to assist the animal health industry.〔1 Board of Agriculture, The Use of Drugs in Food Animals: Benefits and Risks. The National Academies Press. 1999. February 2010. Page 99.
==Overview==
The Animal Drug Availability Act specifies the conditions in which the U.S. Secretary of Health can refuse the application of a new drug. The possibility of an unconsidered hazard is not a permitted ground for refusing an application.
The implications of the act include:
* more relaxed controls on field studies unless requested and justified by the Center for Veterinary Medicine;
* a strict demand for proof of efficacy;
* a definition of adequate and well controlled procedures for field trials;
* supporting labeling focused on the range of recommended or acceptable dosages;
* creating veterinary feed directive drugs as a new category of animal drugs.〔Board of Agriculture, The Use of Drugs in Food Animals: Benefits and Risks. The National Academies Press. 1999. February 2010. Page 99.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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