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PDA技术报告总目录（2015年官网更新） 1. Validation of Moist Heat Sterilization Processes: Cycle Design, Development, Qualification and Ongoing Control Revised 2007 (Published 1980) 湿热灭菌工艺验证：循环设计、研发、确认和持续控制，修订2007 3. Validation of Dry Heat Processes Used for Depyrogenation and Sterilization Revised 2013 (Published 1981) 01003 43506 用于除热源和灭菌的干热工艺验证，修订2013 4. Design Concepts for the Validation of Water-for-Injection Systems 1983注射用水系统验证的设计概念，1983 5. Sterile Pharmaceutical Packaging: Compatibility and Stability 1984 无菌制剂包装：相容性和稳定性，1984 7. Depyrogenation 1985 除热源，1985 9. Review of Commercially Available Particulate Measurement Systems 1988商业可采购的颗粒物检测系统审核，1988 10. Parenteral Formulations of Proteins and Peptides: Stability and Stabilizers 1988 蛋白质和多肽注射制剂：稳定性和稳定剂，1988 11. Sterilization of Parenterals by Gamma Radiation 1988 静脉注射伽马辐射灭菌，1988 12. Siliconization of Parenteral Drug Packaging Components 1988 静脉注射剂药品包装组分硅化处理，1988 13. Fundamentals of an Environmental Monitoring Program Revised 2014 (Published 1990) 环境监测计划原则，修订2014 14. Validation of Column-Based Chromatography Processes for the Purification of Proteins Revised 2008 (Published 1992) 蛋白纯化用柱色谱工艺验证，修订2008 15. Validation of Tangential Flow Filtration in Biopharmaceutical Applications Revised 2009 (Published 1992) 生物制药用正切流过滤验证，修订2009 16. Effect of Gamma Irradiation on Elastomeric Closures 1992 人造橡胶塞伽马辐射效应，1992 17. Current Practices in the Validation of Aseptic Processing -- 1992 1993 无菌工艺验证现行规范，1992，1993 18. Report on the Validation of Computer-Related Systems 1995 计算机相关系统验证报告，1995 19. Rapid/Automated ID Methods Survey 1990 快速/自动ID方法调查，1990 20. Report on Survey of Current Industry Gowning Practices 1990 行业现行更衣规范调查报告，1990 21. Bioburden Recovery Validation 1990 生物负载回收率验证，1990 22. Process Simulation for Aseptically Filled Products Revised 2011 (Published 1996) 无菌药品模拟工艺灌装，修订2011 23. Industry Survey on Current Sterile Filtration Practices 1996 现行无菌过滤实践行业调查，1996 24. Current Practices in the Validation of Aseptic Processing – 1996 1996 无菌工艺验证现行规范，1996 25. Blend Uniformity Analysis: Validation and In-Process Testing 1997 混合均一性分析：验证和中控测试，1997 26. Sterilizing Filtration of Liquids Revised 2008 (Published 1998) 液体无菌过滤，修订2008 27. Pharmaceutical Package Integrity 1998药品包装完整性，1998 28. Process Simulation Testing for Sterile Bulk Pharmaceutical Chemicals Revised 2006 (Published 1998) 无菌API模拟工艺灌装，修订2006 29. Points to Consider for Cleaning Validation Revised 2012 (Published 1998) 清洁验证的考虑要点，修订2012 30. Parametric Release of Pharmaceuticals and Medical Device Products Terminally Sterilized by Moist Heat Revised 2012 (Published 1999) 最终湿热灭菌的药物和医疗器械参数放行，修订2012 31. Validation and Qualification of Computerized Laboratory Data Acquisition Systems 1999 计算机化实验室数据获取系统验证和确认，1999 32. Auditing of Suppliers Providing Computer Products and Services for Regulated Pharmaceutical Operations Revised 2004 (Published 1999) 提供受法规管理的药物操作用计算机产品和服务的供应商审计，修订2004 33. Evaluation, Validation and Implementation of Alternative and Rapid Microbiological Methods Revised 2013 (Published 2000) 替代性和快速微生物方法的评估、验证和实施，修订2013 34. Design and Validation of Isolate Systems for the Manufacturing and Testing of Health Care Products 2001 保健药品的生产和检测分离系统的设计和验证，2001 35. A Proposed Training Model for the Microbiological Function in the Pharmaceutical Industry 2001制药行业微生物功能培训模式建议，2001 36. Current Practices in the Validation of Aseptic Processing – 2001 2002 无菌工艺验证现行规范--2001，2002 38. Manufacturing Chromatography Systems Post-Approval Changes: (ChromPAC):Chemistry, Manufacturing and Controls Documentation 2006 批准后生产用色谱系统：研发、生产和控制文件，2006 39. Guidance for Temperature-Controlled Medicinal Products: Maintaining the Quality of Temperature-Sensitive Medicinal Products through the Transportation Environment 2007 温度受控药物指南：通过运输环境来维护对温度敏感的药物的质量，2007 40. Sterilization Filtration of Gases 2005 气体的无菌过滤，2005 41. Virus Filtration 2008 病毒过滤，2008 42. Process Validation of Protein Manufacturing 2005 蛋白质生产的工艺验证，2005 43. Identification and Classification of Nonconformities in Molded and Tubular Glass Containers for Pharmaceutical Manufacturing Revised 2013 (Published 2007) 药物生产用模型制备和管式玻璃容器的识别和分类，修订2013 44. Quality Risk Management for Aseptic Processes 2008 无菌工艺的质量风险管理，2008 45. Filtration of Liquids Using Cellulose-Based Depth Filters 2008 使用纤维素基础深层过滤器的液体过滤，2008 46. Last Mile: Guidance for Good Distribution Practices for Pharmaceutical Products to the End User 2009最终里程：给最终用户的药物优良销售规范指南，2009 47. Preparation of Virus Spikes Used for Virus Clearance Studies 2010 用于病毒清除研究的病毒加标样制备，2010 48. Moist Heat Sterilizer Systems: Design, Commissioning, Operation, Qualification and Maintenance 2010 湿热灭菌系统：设计、调试、运行、确认和维护，2010 49. Points to Consider for Biotechnology Cleaning Validation 2010 生物制品清洁验证考虑要点，2010 50. Alternative Methods for Mycoplasma Testing 2010 支原体测试替代性方法，2010 51. Biological Indicators for Gas and Vapor-Phase Decontamination Processes: Specification, Manufacture, Control and Use 2010 气体和蒸汽相除污染工艺生物指示剂：质量标准、生产、控制和使用，2010 52. Guidance Good Distribution Practices for the Pharmaceutical Supply Chain 2011 药品供应链优良销售规范指南，2011 53. Guidance for Industry: Stability Testing to Support Distribution of New Drug Products 2011 行业指南：支持新药销售的稳定性测试，2011 54. Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations 2012 药品和生物制品生产操作的质量风险管理实施，2012 54-2. Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operation: Annex 1: Case Study Examples for Quality Risk Management in Packaging and Labeling 2013 药品和生物制品生产操作的质量风险管理实施，附录1：包装和标识中的质量风险管理案例研究，2013 54-3. Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations Annex 2: Case Studies in the Manufacturing of Pharmaceutical Drug Products 2013药品和生物制品生产操作的质量风险管理实施，附录2：药品生产中的质量风险管理案例研究，2013 54-4. Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations Annex 3: Case Studies in the Manufacturing of Biotechnological Bulk Drug Substances 2015 药品和生物制品生产操作的质量风险管理实施，附录3：生物散装药用物质生产中的质量风险管理案例研究，2013 55. Detection and Mitigation of 2,4,6-Tribromoanisole and 2,4,6-Trichloroanisole Taints and Odors in the Pharmaceutical and Consumer Healthcare Industries 2012 药物和保健行业中2，4，6-三溴苯甲醚和2，4，6-三氯苯甲醚污染和气味的检测和移除，2012 56. Application of Phase-Appropriate Quality Systems and CGMP to the Development of Therapeutic Protein Drug Substance 2012 治疗用蛋白质药用物质研发中与阶段相适当的质量体系和CGMP应用，2012 57. Analytical Method Validation and Transfer for Biotechnology Products 2012 生物制品的分析方法验证和转移，2012 58. Risk Management for Temperature-Controlled Distribution 2012 温度受控销售风险管理，2012 59. Utilization of Statistical Methods for Production Monitoring 2012 生产监测用统计学方法使用，2012 60. Process Validation: A Lifecycle Approach 2013 工艺验证：生命周期方法，2013 61. Steam In Place 2013 在线蒸汽，2013 62. Recommended Practices for Manual Aseptic Processes 2013人工无菌工艺规范建议，2013 63. Quality Requirements for the Extemporaneous Preparation of Clinical Trial 2013 临床试验临时制备药物的质量要求，2013 64. Active Temperature-Controlled Systems: Qualification Guidance 2013 在用温度控制系统：确认指南，2013 65. Technology Transfer 2014 技术转移，2014 66. Application of Single-Use Systems in Pharmaceutical Manufacturing 2014 药物生产中单次使用系统的应用，2014 67. Exclusion of Objectionable Microorganisms from Nonsterile Pharmaceuticals, Medical Devices, and Cosmetics 2014 非无菌药物、医疗器械和化妆品中致病菌排除，2014 68. Risk-Based Approach for Prevention and Management of Drug Shortages 2014 基于风险的药品存贮预防和管理，2014 73.Prefilled Syringe User Requirements for Biotechnology Applications预灌封注射器用户要求对生物技术的应用 后续我会继续关注PDA网站，如果更新我会继续补充，希望大家回帖支持我
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