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中药制剂清洁验证探讨 被引量:6

Approaches to Cleaning Validation of Traditional Chinese Medicines
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摘要 通过对中药制剂特点及清洁验证中难点的分析,探讨适合中药制剂清洁验证的方法。提出结合目视法、电导率法和总有机碳(TOC)法制定可行、有效的中药制剂清洁验证方案,为中药制剂生产企业GMP清洁验证工作提供参考。
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2015年第8期925-928,共4页 Chinese Journal of Pharmaceuticals
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参考文献14

  • 1Pluta P. The top4 cleaning validation problems [EB/OL].[2013-10-30]. http://www.ivtnetwork.com/article/top-4-cleaning-validation-problems.
  • 2US Food and Drug Administration. Guide to inspectionsvalidation of cleaning processes [EB/OL]. [2014-11-25].http://www.fda.gov/ICECI/Inspections/InspectionGuides/ucm074922.htm.
  • 3Mendenhall DW. Cleaning validation [J]. Drug Dev IndPharm, 1989,15(13):2015-2114.
  • 4LeBlanc DA. "Visually clean" as a sole acceptance criterionfor cleaning validation protocols [J]. FDA J Pharm SciTechnol, 2002, 56(1): 31-36.
  • 5Forsyth RJ, Nostrand VV. Application of visible residue limitfor cleaning validation in a pharmaceutical manufacturingfacility[J].Pharm Technol, 2005, 29(10): 152-161.
  • 6Forsyth RJ, Nostrand VV, Martin GP. Visible-residue limitfor cleaning validation and its potential application in apharmaceutical research facility [J]. Pharm Technol, 2004,28(10): 58-72.
  • 7张根生.电滲析水处理技术[M]. 1版,北京:科学出版社,1981: 10-13.
  • 8刘瑞轩,干爱华,王韬,张敬,孙永利,李鑫钢.电生物膜处理含重金属离子废水的浓度在线检测方法[J].西南给排水,2005,27(4):36-39. 被引量:2
  • 9冯常泗,赵殿明.实施GMP过程中管路系统的清洁验证[J].山东医药工业,2002,21(6):41-42. 被引量:3
  • 10徐飞,张志华,李晶玉,艾萍.TOC检测法测定羟乙基淀粉200/0.5残留量[J].齐鲁药事,2012,31(7):410-411. 被引量:1

二级参考文献21

  • 1[5]D A LeBlanc.Establishing Scientifically Justified Acceptance Criteria for Cleaning Validation of Finished Drug Products[J].Pharmaceutical Technology,1998,22(10):136-148.
  • 2[6]Sherwood,David,Clifford J,et al.Experiences with clean-in-place validation in a multiProduct biopharmaceutical manufacturing facility[J].Eunpean Journal of Parenteral Science,1996,2(1):35-41.
  • 3[1]U S FDA(1993).Guide to inspections of validation of cleaning processes[S].
  • 4[2]U S FDA(1992).Mid Atlantic Region inspection Guide on cleaning validation[S].
  • 5[3]Four,Gary L,Mullen,Michael V.Determining cleaning validation acceptance limits for pharmaceutical manufacturing operations[J].Pharmaceutical Technology,1993,17(4):54-60.
  • 6[4]Vincent,David W.Cleaning validation for the biotechnology and biological industries-part Ⅱ[J].Journal of Validation Technology,2000,6(4):706-723.
  • 7Li Tiancheng, Jiang Bin, Wang Dawei, Yuan Shaojun, Feng Xia.Purification of organic wa.etewater containing heavy metal ions by a combined process of micro electTolysis and biofilm[ J]. Chinese Journal of Chemical Engineering.
  • 8Li Tiancheng, Li 'Xingang, Feng Xia, Jiang Bin, Wand Dawei, Yuan Shaojun. Treatment of organic wastewater containing Cr^3+ by a novel complex process of electrodeposifion and biofilm [ J ]. Transactions of Tianjin University.
  • 9宋世谟 王正烈 李文斌.物理化学[M]第三版[M].北京:高等教育出版社,1997.17-22.
  • 10张根生.电渗析处理技术(第一版)[M].北京:科学出版社,1981.10-13.

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