最新pda技术报告
：报告最新技术p da pda技术报告清单2016 pda技术报告是什么pda技术报告灭菌决策树
篇一：PDA技术报告清单2015
PDA技术报告清单（官网2015年更新）
store.pda/ProductCatalog/ProductCategory.aspx?ID=30 1. Validation of Moist Heat Sterilization Process: Cycle Design, Development, Qualification and Ongoing Control Revid 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 Process Ud for Depyrogenation and Sterilization Revid 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小学英语试卷
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 Revid 2014 (Published
1990)
环境监测计划原则，修订2014
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14. Validation of Column-Bad Chromatography Process for the Purification of Proteins Revid 2008 (Published 1992)
代词是什么蛋白纯化用柱色谱工艺验证，修订2008
pending
15. Validation of Tangential Flow Filtration in Biopharmaceutical Applications Revid 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 Aptic Processing -- 1992 1993 无菌工艺验证现行规范，1
992，1993
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
build是什么意思生物负载回收率验证，1990
22. Process Simulation for Aptically Filled Products Revid 2011 (Published 1996) 无菌灌装药品工艺模拟，修订2011
explain23. 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 Aptic Processing –1996 1996公主日记1
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
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26. Sterilizing Filtration of Liquids Revid 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 Revid 2006 (Published 1998)
无菌散装药用化学物工艺模拟测试，修订2006
29. Points to Consider for Cleaning Validation Revid 2012 (Published 1998) 清洁验证的考虑要点，修订2012
30. Parametric Relea of Pharmaceuticals and Medical Device Products Terminally Sterilized by Moist Heat Revid 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 Revid 2004 (Published 1999)
石家庄43中
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 Revid 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 Propod Training Model for the Microbiological Function in the
Pharmaceutical Industry 2001
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制药行业微生物功能培训模式建议，2001
36. Current Practices in the Validation of Aptic Processing –2001 2002 无菌工艺验证的现行规范--2001，2002
38. Manufacturing Chromatography Systems Post-Approval Changes:
考研英语作文范文
(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失败英文
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
