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《联邦杀虫剂、杀菌剂和杀鼠剂法案》-88、良好实验室规范和质量保证:农药注册。

FIFRA-88, GLP, and QA: pesticide registration.

作者信息

Sterner R T, Fagerstone K A

机构信息

USDA/APHIS/WS, National Wildlife Research Center, Ft. Collins, Colorado 80524-2719, USA.

出版信息

Qual Assur. 1997 Jul-Sep;5(3):171-82.

PMID:9509549
Abstract

The 1988 amendment to the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA-88) has decreased the number of pesticide registrations in the United States. Subsequent implementation of the U.S. Environmental Protection Agency (EPA) Good Laboratory Practice (GLP) and quality assurance (QA) standards has increased costs of maintaining these registrations. The U.S. Department of Agriculture (USDA) Animal and Plant Health Inspection Service (APHIS) maintains approximately 30 Section 3 (federal) or Section 24c (state) vertebrate pesticide registrations for the Wildlife Services (WS) program to control wild mammals and birds that damage crops, impact endangered species, or pose human health risks. Under FIFRA-88, APHIS summarized, performed, and submitted or gained waivers for > 500 studies requested by the U.S. EPA to assess potential hazards/effects of these pesticides. A summary of FIFRA-88 milestones for registration of 3-chloro-p-toluidine hydrochloride (CPTH), the active ingredient (AI) in a "low-volume, minor-use" avicide (DRC-1339, Starlicide), is used to illustrate GLP/QA/animal welfare issues involved in this process. Trends in the development of new pesticides and veterinary drugs are compared to provide some perspectives on future career paths for QA professionals.

摘要

1988年对《联邦杀虫剂、杀菌剂和杀鼠剂法案》(FIFRA - 88)的修订减少了美国农药注册的数量。随后美国环境保护局(EPA)良好实验室规范(GLP)和质量保证(QA)标准的实施增加了维持这些注册的成本。美国农业部(USDA)动植物卫生检验局(APHIS)为野生动物服务(WS)项目维持了约30项第3条(联邦)或第24c条(州)脊椎动物农药注册,以控制对农作物造成损害、影响濒危物种或构成人类健康风险的野生哺乳动物和鸟类。根据FIFRA - 88,APHIS总结、开展并提交了美国EPA要求的500多项研究,或获得了这些研究的豁免,以评估这些农药的潜在危害/影响。以“低容量、小用量”杀鸟剂(DRC - 1339,Starlicide)中的活性成分3 - 氯 - 对甲苯胺盐酸盐(CPTH)注册的FIFRA - 88里程碑总结为例,来说明这一过程中涉及的GLP/QA/动物福利问题。比较了新农药和兽药的发展趋势,为QA专业人员的未来职业道路提供一些视角。

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