期刊文献+

我国GLP建设与实施的几点问题和建议 被引量:5

On formulating and implementing GLP in China
下载PDF
导出
摘要 阐述我国GLP建设和实施的现状,在实施过程中应防止出现的问题,提出加强政府引导和监管、正确认识GLP的建设和实施、GLP管理方面的几点建议。 This article illustrates the actual status of formulation and implementation of GLP in China, proposes preventive measures for probable issues which may occur in the process of GLP implementation, and gives suggestions on enhancing authorities guidance and supervision of GLP formulation and implementation, understanding and administrating GLP.
作者 叶有春
出处 《安徽医药》 CAS 2006年第5期388-389,共2页 Anhui Medical and Pharmaceutical Journal
关键词 GLP建设和实施 GLP管理 质量管理 软硬件 GLP formulation and implementation GLP management quality management software and hardware
  • 相关文献

参考文献1

二级参考文献5

  • 11,Harston SJ,Pharm B, ScM.Implementation of good laboratory practices by european pharmaceutical companies. DrugInformation Journal, 1994,28:1055
  • 22,International Conference on Harmonization.Toxicokinetica:the assessment of systemicexposure in toxicity studies. Draft guideline of 1993
  • 33,Fleischhauer H.The cost of GLP compliance. Pharmaceutical Technology, 1984 January:26
  • 44,Hembeck HW. GLP Harmonization in the European Community: GLP inspection versus studyaudit. Drug Information Journal, 1994,28:1081
  • 55,OECD.Good laboratory practice in the testing of chemicals:Final report of the group ofexperts on good laboratory practice

共引文献8

同被引文献35

引证文献5

二级引证文献30

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部