WHOTechnicalReportSeries,No.957,2010 Annex1 WHOgoodpracticesforpharmaceutical qualitycontrollaboratories Generalconsiderations Glossary Partone.Managementandinfrastructure 1.Organizationandmanagement 2.Qualitymanagementsystem 3.Controlofdocumentation 4.Records
WHO_OOS_gpcl_trs957_annex1 热度: 药品生产管理规范论文 热度: 2、2010版药品GMP生产管理讲义 热度: Annex3 WHOgoodmanufacturingpracticesfor pharmaceuticalproductscontaininghazardous substances 附录3 含毒质药品WHO生产管理规范 1.Introduction 2.General
Annex 3 WHO good manufacturing practices for pharmaceutical products containing hazardous substances 附录3 含毒质药品WHO生产管理规范 1. Introduction 2. General 3. Glossary 4. Risk assessment 5. Product protection 6. Personal protection equipment and breathing air systems 7. Environmental protection 8. ...
eu gmp annex 11 中文 WHO GMP Sterile 2010 Annex 4 TRS957_2010.doc,eu gmp annex 11 中文 WHO GMP Sterile 2010 Annex 4 TRS957_2010 导读:就爱阅读网友为您分享以下“WHO GMP Sterile 2010 Annex 4 TRS957_2010”的资讯,希望对您有所帮助,感谢您对92的支持! Table 2
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 ...
2011-1-18 主要内容 一、WHO预认证简介 二、WHOGPCL简介 三、中检院化学药品实验室预认证情况 四、WHO预认证及药品抽验相关实验室区域间研讨会五、全国药检系统质量管理体系建设 一、WHO预认证简介 •WHO预认证的目的 –增加质控实验室的数量：符合药品检验的相关标准并受委托为联合国机构进行药品检验；–...
WHO TRS 1022 第55 次 报告 Annex 3 Good manufacturing practices: water for pharmaceutical use 优良生产规范( GMP ): 制药用水 Background 背景 Unlike other product or process ingredients, water is usually drawn from an on demand system and is not subject to testing and batch or lot release ...
Annex5 Guidanceongooddataandrecordmanagementpractices Background Duringaninformalconsultationoninspection,goodmanufacturingpractices andriskmanagementguidanceinmedicines’manufacturingheldbythe WorldHealthOrganization(WHO)inGenevainApril2014,aproposalfor newguidanceongooddatamanagementwasdiscussedanditsdevelopment ...
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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...