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Report on Progress Made towards GLP Compliance in China

机译:报告中国GLP遵从性的进展

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摘要

@@ 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:@@良好的实验室练习(GLP)是一个有关的质量系统,有关组织过程以及在实验室,温室和该领域的非临床健康和环境安全研究的条件是计划,进行,监测,记录,存档和报道。 GLP适用于法规所要求的测试项目的非临床安全测试,以便登记或授权药物,农药,食品和饲料添加剂,化妆品,兽医药品和类似产品,以及工业化学品的调节。

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