TR 30 2012 | 最终湿热灭菌的药物和医疗器械参数放行
Parametric Release of Pharmaceuticals and Medical Device Products Terminally Sterilized by Moist Heat |
TR 39 Rev-2021 | 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
Guidance for Temperature-Controlled Medicinal Products: Maintaining the Quality of Temperature-Sensitive Medicinal Products through the Transportation Environment |
TR 41 Rev-2022 | 病毒过滤
Virus Filtration |
TR 43 Rev-2013 | 药物生产用模型制备和管式玻璃容器的识别和分类
Identification and Classification of Nonconformities in Molded and Tubular Glass Containers for Pharmaceutical Manufacturing: Covering Ampoules, Bottles,Cartridges, Syringes and Vials |
TR 46 2009 | 最终里程:给最终用户的药物优良销售规范指南
Last Mile: Guidance for Good Distribution Practices for Pharmaceutical Products to the End User |
TR 50 2010 | 支原体测试替代性方法
Alternative Methods for Mycoplasma Testing |
TR 53 2011 | 行业指南:支持新药销售的稳定性测试
Guidance for Industry: Stability Testing to Support Distribution of New Drug Products |
TR 54-6 2019 | 赋形剂的正式风险评估
Formalized Risk Assessment for Excipients |
TR 55 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
Detection and Mitigation of 2,4,6-Tribromoanisole and 2,4,6-Trichloroanisole Taints and Odors in the Pharmaceutical and Consumer Healthcare Industries |
TR 57-2 | 生物技术产品的分析方法开发和鉴定
Analytical Method Development and Qualification for Biotechnology Products |
TR 63 2013 | 临床试验临时制备药物的质量要求
Quality Requirements for the Extemporaneous Preparation of Clinical Trial Materials |
TR 67 2014 | 非无菌药物、医疗器械和化妆品中致病菌排除
Exclusion of Objectionable Microorganisms from Nonsterile Pharmaceuticals,Medical Devices, and Cosmetics |
TR 71 2015 | 病毒检测的新方法
Emerging Methods for Virus Detection |
TR 72 2015 | 全球销售控温药品的防热保护系统 :确认与操作指南
Passive Thermal Protection Systems for Global Distribution: Qualification and Operational Guidance |