Comparison on features of "Good Laboratory Practice for Nonclinical Laboratory Studies" among USA,OECD and China

LIU Xia; YE Hua

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Volume 26 Issue 5

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Article Navigation > Journal of Pharmaceutical Practice and Service > 2008 > (5): 372-375

LIU Xia, YE Hua. Comparison on features of 'Good Laboratory Practice for Nonclinical Laboratory Studies' among USA,OECD and China[J]. Journal of Pharmaceutical Practice and Service, 2008, (5): 372-375.

Citation:

LIU Xia, YE Hua. Comparison on features of "Good Laboratory Practice for Nonclinical Laboratory Studies" among USA,OECD and China[J]. Journal of Pharmaceutical Practice and Service, 2008, (5): 372-375.

Comparison on features of "Good Laboratory Practice for Nonclinical Laboratory Studies" among USA,OECD and China

LIU Xia,
YE Hua

School of Pharmacy,Fudan University,Shanghai 200032,China

Received Date: 2007-09-12

Abstract

According to the comparison on the items in three GLP(/or Principle)formed by USA,OECD and China,respective- ly,and on their foundation,history and current status,the advantages of each GLP(/or Principle)have been studied.Some advices are presented,which are actualizing GLP needs consummate law and supervise system;making the full use of QAU;establishing the e- lectric collection system of test data.It is also a developing course.
- drug safety evaluation,
- GLP,
- USA,
- OECD
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通讯作者: 陈斌, bchen63@163.com

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沈阳化工大学材料科学与工程学院沈阳 110142

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