随着新药安全性评价研究工作的蓬勃开展,我国期刊杂志介绍国外GLP工作的文章逐年增多,现结合对这一法规和各国GLP的理解,将其中常用术语的定义介绍如下:1 药品非临床研究质量管理规定(good laboratory practicefor non-clinical laboratory studies,GLP):是实验室研究在计划、执行、监督、记录和报告方面的组织过程和条件。(也 With the vigorous development of new drug safety evaluation research, our country journals and magazines introduce the work of foreign GLP articles increasing year by year, now combined with the understanding of this regulation and GLP of each country, the definitions of commonly used terms are introduced as follows: 1 Non-clinical study of drugs Good laboratory practice for non-clinical laboratory studies (GLP): is a laboratory study of organizational processes and conditions in planning, implementing, monitoring, recording and reporting. (and also