who_trs_908-annex9 热度: 相关推荐 59 ©WorldHealthOrganization WHOTechnicalReportSeries,No.929,2005 Annex4 WHOguidelinesforsamplingofpharmaceutical productsandrelatedmaterials 1.Introduction61 1.1Generalconsiderations61 1.2Glossary61 1.3Purposeofsampling64 1.4Classesandtypesofpharmaceuticalproductsandrelated mat...
59© World Health OrganizationWHO Technical Report Series, No. 929, 2005Annex 4WHO guidelines for sampling of pharmaceuticalproducts and related materials1.Introduction1.1General considerations1.2Glossary1.3Purpose of sampling1.4Classes and types of pharmaceutical products and relatedmaterials1.5Sampling facilit...
Annex5 Guidanceongooddataandrecordmanagementpractices Background Duringaninformalconsultationoninspection,goodmanufacturingpractices andriskmanagementguidanceinmedicines’manufacturingheldbythe WorldHealthOrganization(WHO)inGenevainApril2014,aproposalfor newguidanceongooddatamanagementwasdiscussedanditsdevelopment ...
WHO_TRS_961 Annex2WHO药品微生物实验室管理规范 下载积分: 1000 内容提示: WHO 技术指南报告 No. 961, 2011, annex 2 WHO 药品微生物实验室管理规范 1 of 27 © World Health Organization 世界卫生组织 WHO Technical Report Series, No. 961, 2011 世界卫生组织技术报告系列,编号961 ,2011 年 Annex 2 ...
Annex4 Supplementaryguidelinesongoodmanufacturing practices:validation 1.Introduction 2.Scope 3.Glossary 4.Relationshipbetweenvalidationandqualification 5.Validation 5.1.Approachestovalidation 5.2.Scopeofvalidation 6.Qualification 7.Calibrationandverification ...
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961, 2011, annex 7 WHO 药品生产技术转移的指导原则 1 of 32 © World Health Organization 世界卫生组织 WHO Technical Report Series, No. 961, 2011 世界卫生组织技术报告系列,编号 961, 2011 年 Annex 7 附录 7 WHO guidelines on transfer of technology in pharmaceutical manufacturing WHO 药品生产技术...
WHO_TRS_961 Annex3 WHO GMP主要原理介绍.pdf,WHO GMP for pharmaceutical products: main principles WHO 技术指南报告No. 961, 2011, annex 3 WHO 药品GMP 主要原理 © World Health Organization WHO Technical Report Series, No. 961, 2011 世界卫生组织技术报告系列
WHO Technical Report Series, No. 970, 2012 Annex 2 附件2Page 1 of 20 Annex 2 附件2 WHO good manufacturing practices: water for pharmaceutical use WHO GMP：制药用水 1. Introduction 介绍 1.1 Scope of the document文件范围 1.2 Background to water requirements and uses 水的要求和使用背景...
908, 2003Annex 9Guide to good storage practices forpharmaceuticals11.Introduction1252.Glossary1263.Personnel1284.Premises and facilities1285.Storage requirements1316.Returned goods1337.Dispatch and transport1338.Product recall134References134Bibliography134Appendix136Storage and labelling conditions1.IntroductionThis ...