Report on Progress Made towards GLP Compliance in China

机译：中国遵守GLP的进展报告

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@@ Good Laboratory Practice (GLP) is a quality system concerned with the organizational process and the conditions under which non-clinical health and environmental safety studies in the laboratory, greenhouses, and the field are planned, performed, monitored, recorded, archived and reported. GLP is applied to the non-clinical safety testing of test items required by regulations for the purpose of registering or licensing pharmaceuticals, pesticides, food and feed additives, cosmetic products, veterinary drug products and similar products, and for the regulation of industrial chemicals.

机译：@@优良实验室规范（GLP）是一种质量体系，与组织过程和条件相关，在该条件下，计划，执行，监控，记录，归档和存档实验室，温室和田间的非临床健康和环境安全研究报告。 GLP适用于法规要求的测试项目的非临床安全性测试，目的是注册或许可药品，农药，食品和饲料添加剂，化妆品，兽药产品及类似产品的注册或许可，以及工业化学品的法规。

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来源
《Proceedings of 4th international symposium on pesticides and environmental safety amp; 5th pan Pacific confernce on pesticide science amp; 8th international workshop on crop protection chemistry and regulatory harmonization》|2012年|38-39|共2页
会议地点 Beijing(CN)
作者
Tiechun Chen;
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作者单位

ICAMA, Beijing, China;

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会议组织
原文格式 PDF
正文语种 eng
中图分类植物化学保护理论;农用化学物质、有毒化学物质污染及其防治;
关键词
pesticides; GLP; management;

机译：农药; GLP;管理;

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Report on Progress Made towards GLP Compliance in China

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