摘要
目的规范供试品管理,使其符合《药物非临床研究质量管理规范》(Good Laboratory Practice,GLP)的要求。方法查找供试品管理各环节存在的问题。结果分析总结了保管、配制、分析等主要环节较易出现的问题并提出意见和建议。结论通过完善供试品管理,关注每一环节的细节操作,真正实现了供试品的有效管理。
Objective To meet the requirements of GLP （Good Laboratory Practice） in the administration of test article. Methods The problems existed in the administration of the test article were searched. Results The problems which might appear in the process of storage, dispensing and analyzing were analyzed and summarized, and some suggestions were put forward. Conclusion By improving the administration of the test article, and concerning about every detail in the operation, effective administration of the test article could be achieved.
出处
《中国药事》
CAS
2014年第2期156-157,共2页
Chinese Pharmaceutical Affairs
