1)drug GMP药品GMP
1.Reviewing the basic situation of Chinese GMP,based on an analysis of the characteristics and the present situation of international drug GMP,for reference on the agreement between Chinese drug GMP and the international standards.在回顾我国实施GMP的基本情况基础上,分析了国际药品GMP的现状与特点,为实现我国药品GMP与国际先进水平接轨提供参考。
2.According to deployment of SFDA, State Food And Drug Administration Center for Certification of Drug and the relevant units and experts, translated the drug GMP regulations and related information of WHO,FDA, EU, Japan, ICH, drugs inspection treaty / Planning Organization (PIC/S) and other countries and organizations.根据国家食品药品监督管理局部署,局药品安全监管司组织药品认证管理中心及有关单位和专家,翻译查阅了世界卫生组织(WHO)、美国食品药品管理局(US-FDA)、欧盟(EU)、日本(JAP)、人用药品注册技术要求国际协调会(ICH)、药品检查条约/合作计划组织(PIC/S)等国家和组织的药品GMP管理法规及相关资料,以我国药品GMP为背景,在管理体系和药品GMP具体内容上进行了对比调研。
英文短句/例句
1.The Developing History of Drug s GMP and the Working Programme of Practicing GMP;药品GMP发展史及实施GMP的工作程序
2.The analysis of the implementation of pharmaceutical GMP model on specie-specific patterns浅析以品种为单元的药品GMP实施模式
3.Research on Implement and Development of Good Manufacturing Practice of Drug in China in New Era;新时期我国药品GMP实施与发展研究
4.Contrast Research Report of Domestic and Foreign Drug GMP (2);国内外药品GMP对比调研报告(二)
5.Contrast Research Report of Domestic and Foreign Drug GMP (1);国内外药品GMP对比调研报告(一)
6.Study on the Economy-law Effects of the Good Manufacturing Practice(GMP) for Drugs in China;对我国药品GMP认证的经济法思考
7.Update of Concept is important to better implementation of GMP深入实施药品GMP管理贵在观念更新
8.Pay Close Attention to the Anew Authentication of Drugs GMP重视和做好药品GMP重新认证工作
9.The Brief Analysis of Risk and Legal Liability of Drug GMP Certification药品GMP认证的风险及法律责任浅析
10.Contrast Research Report of Domestic and Foreign Drug GMP(5～6)国内外药品GMP对比调研报告(五～六)
11.Contrast Research Report of Domestic and Foreign Drug GMP (4)国内外药品GMP对比调研报告(四)
12.The Problems Which Should be Especially Concerned in Drug GMP Authentic Examination;药品GMP认证现场检查时应特别关注的问题
13.Study the trend of materials management according to the revision of China's GMP of Drugs从我国药品GMP的修订看物料管理的动向
14.Application of quality risk management (QRM) in drug GMP site inspection质量风险管理在药品GMP现场检查中运用的探讨
15.Ideas and Prospects of Application of Remote Diagnosis and Distance Education in the Management of GMP;远程诊断和远程教育在药品GMP管理中应用的设想与展望
16.The Study of Pharmaceutical Enterprise Drawing Lessons from TQM to Consummate GMP;药品生产企业借鉴TQM完善GMP研究
17.Main Differences between GMP Requirements of EU and Non-bacteria Drug Production in China;我国无菌药品生产与欧盟GMP要求的主要不同点
18.Discussion on the Methods and Skills for Implementation of GMP Self Inspection in the Drug Production Enterprises;浅谈药品生产企业实施GMP自检的方法和技巧
相关短句/例句
drug GMP certification药品GMP认证
1.Objective To propose that should adopt some evasion risk methods in the drug GMP certification process.目的提出了在药品GMP认证过程中应采取的一些规避风险的方法。
3)Drug GMP management药品GMP管理
4)good manufacture practice (GMP) or good radiopharmacy practice (GRP)药品生产管理规范(GMP/GRP)
5)Veterinary drug GMP兽药GMP
1.The intermingle of good and bad in enterprise management, however, result in problems of veterinary drug GMP quality management system when it works.兽用生物制品生产企业实施兽药GMP管理是提高竞争力和产品质量的有效途径。
6)GMP compliance standard药品GMP认证检查评定标准
延伸阅读
非法提供麻醉药品、精神药品罪非法提供麻醉药品、精神药品罪：指依法从事生产、运输、管理、使用国家管制的麻醉药品、精神药品的单位和个人，明知他人是吸毒者，而向其提供国家管制的能够使人成瘾的麻醉药品、精神药品的行为。
