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刊物信息

期刊名称:药物分析杂志
主管单位:中国科学技术协会
主办单位:中国药学会
承办:中国食品药品检定研究院
主编:金少鸿
地址:北京天坛西里2号
邮政编码:100050
电话:010-67012819,67058427
电子邮箱:ywfx@nifdc.org.cn
国际标准刊号:ISSN 0254-1793
国内统一刊号:CN 11-2224/R
邮发代号:2-237
 

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分析方法确认内容介绍

Analytical method verification in China OMCLs

分类号:
出版年·卷·期(页码):2015,35 (1):0-0
DOI: 10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------

方法确认是药品检验机构在采用药典方法或者法定方法进行检验时必不可少的一个环节.通过合适的方法确认,证明检验人员有能力操作药典方法或法定方法以及证明方法对品种的适用性.目前国内各药品检验所对方法确认的理解不同,做法也不一致.本文根据我国药品检验实际工作内容,结合国际最新指导原则,阐述了药品检验方法确认的概念,给出了药检工作中最常使用的三类检测方法确认需要进行的具体内容,为日常检验工作提供指导.

-----英文摘要:---------------------------------------------------------------------------------------

Analytical method verification is an essential procedure when we employ the compendial or standard method for the quality control of medicines.By performing analytical method verification,the suitability of compendail methods is demonstrated and meanwhile the capability of analysts to successful operate the method is assured.Currently there exists various misunderstandings regarding analytical method verification among China Official Medicine Control Laboratories(OMCLs).This paper elaborates the concept of analytical method verification based on the guidelines available and the daily work of China OMCLs,and more importantly,defines the activities that are required to fulfill method verification for the three most commonly used categories of chemical test methods,eventually to provide a practical guidance for medicine quality control work in China OMCLs.

-----参考文献:---------------------------------------------------------------------------------------
[1] WHO Technical Report Series 937 [S].2006
[2] CNAS Guidance:Accreditation Criteria for the Competence of Testing and Calibration Laboratories(检测和校准实验室能力认可准则) [S].2005
[3] CNAS Guidance:Guidance on the Application of Testing and Calibration Laboratories Competence Accreditation Criteria in the Field of Chemical Testing(检测和校准实验室能力认可准则在化学检测领域的应用说明) [S].2012
[4] ISO/IEC 17025,General Requirements for the Competence of Testing and Calibration Laboratories [S].2005
[5] PA/PH/OMCL(05)47 DEF,Validation of Analytical Procedures,OMCL Network of the Council of Europe Quality Assurance Document [S].1999
[6] USP 32-NF 27 [S].2009:736
[7] AOAC Guidance:How to Meeting ISO 17025 Requirement for Method Verification,Association of Official Analytical Chemists [S].2007
[8] Laboratory of Government Chemist(LGC)Guidance:In-House Method Validation:A Guide for Chemical Laboratories [S].2003
[9] IUPAC Technical Report,Harmonized Guidelines for Single-Laboratory Validation of Method of Analysis [J].Pure Appl Chem,2002,74(5):835
[10] Eurachem Guidance:The Fitness for Purpose of Analytical Methods-A Laboratory Guide to Method Validation and Related Topics [S].1998
[11] CURRIE L.Nomenclature in evaluation of analytical methods,including quantification and detection capabilities [J].Pure Appl Chem,1995,67(8):1699
[12] THOMPSON M,WOOD R.The international harmonized protocol for the proficiency testing of(chemical)analytical laboratories [J].Pure Appl Chem,1993,65(9):2123
[13] THOMPSON M,WOOD R.Harmonized guidelines for internal quality control in alaytical chemistry laboratories [J].Pure Appl Chem,1995,67(4):49
[14] THOMPSON M,ELLISON SRL,FAJGELJ A,et al. Harmonized guidelines for the use of recovery information in alaytical measurement [J].Pure Appl Chem,1999,71(2):337
[15] U.S.FDA-Guidance for Industry:Analytical Procedures and Methods Validation:Chemistry,Manufacturing,and Controls and Documentation [S].2000
[16] U.S.FDA-Guidance for Industry:Bioanalytical Method Validation [S].2001
[17] EMA.Guidance on Validation of Analytical Procedures:Text and Methodology [S].2003
[18] ZHOU HJ(周海钧).Technical Requirements for Registrations of Pharmaceuticals of Human Use(药品注册的国际技术要求) [M].Beijing(北京):People's Medical Publishing House(人民卫生出版社),2006
[19] ChP 2010.Vol Ⅱ(中国药典2010年版.二部) [S].2010:Appendix(附录)194
[20] IP 4 [S].2006
[21] USP 36-NF 31 [S].2013:983,496,510,521
[22] EP 7.1 [S].2011:3
[23] JP 16 [S].2011:2159
[24] GB/T 19000-2000 Quality management systems-fundamentals and terminology(质量管理体系基础和术语) [S].2000
[25] TAN DJ(谭德讲),YANG HX(杨化新),ZHANG HZ(张河战).Understanding of the terms validation,verification and qualification in quality management(对validation,verification和qualification三个质量管理术语之理解) [J].Chin Pharm Aff(中国药事),2013,27(1):22

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