GLP是Good Laboratory Practice的缩写。以往对GLP的含义有不同的理解,有的译为“药品安全性试验规范”,也有的译为“药品生物活性安全性试验规范”。现在通行的译法称“新药非临床安全性研究管理规范”。因为事实上GLP的内容并不包括医药产品研究的全过程,也不包括评价药物安全性的临床试验。其研究管理范围主要是通过体内外测试系统,用细菌、细胞和实验动物来研究药物的毒性(包括全身性毒性),包括对生殖、免 GLP is an acronym for Good Laboratory Practice. In the past the meaning of GLP have different understandings, and some translated as “drug safety test norms”, and some translated as “drug biological safety test norms.” The current translation of the law that “non-clinical drug safety research management practices.” Because in fact the content of GLP does not include the whole process of pharmaceutical product research, nor does it include clinical evaluation of drug safety trials. Its research management mainly through the in vitro and in vitro test system, with bacteria, cells and laboratory animals to study the toxicity of drugs (including systemic toxicity), including reproductive, free