美国药典对残留溶剂的规定_——写自第二届中美药品分析技术与检测方法研讨会___
Regulation of residual solvent in USP ——from China-US joint symposium on pharmaceutical analytical technology and compendial methods
分类号：
出版年·卷·期（页码）：2009,29 (12):0-0
DOI:
10.16155/j.0254-1793.2017.01.01
-----摘要：-------------------------------------------------------------------------------------------
中国药品生物制品检定所与美国药典委员会于于2009年11月6日至8日在广州联合举办了第二届中美药品分析技术与检测方法研讨会，会议主题为“药品质量与生命安全”。本文概述了研讨会关于USP对残留溶剂的有关规定。
-----英文摘要：---------------------------------------------------------------------------------------
China-US Joint Symposium on Pharmaceutical Analytical Technology and Compendial Methods was held in Guangzhou by National Institute for the Control of Pharmaceutical and Biological Products and US Pharmacopoeia Commision. The Regulation of residual solven given by this Forms is reviewed in this paper.
-----参考文献：---------------------------------------------------------------------------------------
1ZHANG Jun-wei（张俊伟）.Review for determination methods of organical residule solevent in drug（药物中有机残留溶剂的测定方法概述）.Mod Instr（现代仪器），2004，3：10
2http://www.usp.org/hottopics/residualSolvents.html
3Guideline for resilual solvent.http://www.ich.org/LOB/media/MEDIA423.pdf
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