1 简介(Introduction) 1.1 目的和范围(Aim and Scope) 1.2 审核手册的制定(Development of an Audit/Inspection Guide) 2 基本信息(如何使用培训手册)[General Information(How to Use This Training Guide)] 2.1 审核培训手册(The Inspection Training Guide) 2.2 审核筹备文件(附录Ⅰ)[Preparatory Documents (Annex I)] 3 审核手册(Inspection Guide) 3.1 注册要求(Licensing Requirements) 3.2 总则 质量体系和质量保证(General Principles-Quality System and Quality Assurance) 3.3 人员及组织机构(Personnel and Organisation) 3.4 场所(Premises) 3.4.1 献血者区域和血液采集区(Blood Donor and Collection Area) 3.4.2 血液检测及血液加工区(Blood Testing and ProcessingArea) 3.4.3 血液储存区(Storage Area Including Blood) 3.4.4 废物处理区(Waste Disposal Area) 3.5 设备及物料(Equipment and Materials) 3.6 文件(Documentation) 3.7 血液采集、检测和加工(Blood Collection,Testing and Processing) 3.7.1 献血者选择(Donor Eligibility) 3.7.2 血液和血液成分采集(Collection of Blood and Blood Components) 3.7.3 实验室检测(Laboratory Testing) 3.7.4 血液加工和验证(Processing and Validation) 3.7.5 贴签(Labelling) 3.7.6 全血和血液成分的发放(Release of Blood and Blood Components) 3.8 储存与配送(Storage and Distribution) 3.9 合同管理(Contract Management) 3.10 不符合项(Non-conformance) 3.11 内部审核、审核及改进(Self-inspection,Audits and Improvements) 3.12 严重不良反应和事件的追溯及通报(Traceability and Notification of Serious Adverse Reactions and Events) 3.13 信息技术(Information Technology) 附录Ⅰ 内部审核流程筹备文件(Preparatory Documentsfor the Self-inspection Process) 附录Ⅱ 互认文件(Documents Cross-referenced) 附录Ⅲ 其他参考资料及相关出版物(Additional References and Project Related Publications) 附录Ⅳ 术语表(Terminology) 附录Ⅴ 项目参与者及合作单位(Project Participants and Collaborating Institutions) 附录Ⅵ 相关或观察机构和参与者(Associated or Observing Institutions and Participants)
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