Good Laboratory Practice(GLP) is conceded with the way laboratory or field studies are planned, monitored, recorded and reported and the conditions under which this occurs. 优良实验室条例涉及实验的设计、监控、记录、报告以及进行上述工作的实验条件。
Study inspection of preclinical safety evaluation of drug is an important responsibility for quality assurance unit ( QAU ) with good laboratory practice ( GLP ). 对新药安全性实验实施质量监督检查是药物非临床研究质量管理规范(GLP)赋予质量保证部门(QAU)的重要职责。
The safety evaluation of drugs refers to drugs non-clinical safety evaluation, or drugs non-clinical research, whose quality management practices are called Good Laboratory Practice(GLP) ( GLP ). 药物安全性评价是指药物非临床安全评价即药物非临床研究,药物非临床研究质量管理规范即GLP。
Comparison Study on Principles of Good Laboratory Practice(GLP) for Non-clinical Studies of Drugs Issued by OECD and SFDA Study on Internationalizing Strategy of Chinese Herbal Medicine and Good Laboratory Practice(GLP) OECDGLP原则与中国GLP规范的比较中药国际化发展战略与GLP的研究