药品GMP认证,drug GMP certification英语短句,例句大全

药品GMP认证,drug GMP certification
1)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。

英文短句/例句

1.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
2.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
3.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
4.Pay Close Attention to the Anew Authentication of Drugs GMP重视和做好药品GMP重新认证工作
5.Analysis on the Instance of GMP Certification Inspection for Beijing Pharmaceutical Manufacturers in 2007;北京市药品生产企业2007年GMP认证检查情况分析
6.Rational Thinking on Achievement of Implementation of GMP and Risks of Drugs Certification对GMP实施成果及药品认证风险的理性思考
7.Analysis of the Main Cause of the Quality of Drugs Existed in Pharmaceutical Manufacturer After Certification of GMP and Countermeasures;浅析GMP认证后药品生产企业存在药品质量问题的主要原因与对策
8.Some Thinking on the Coordination Among GMP Certification,Quality Standard of Drug and Market SupervisionGMP认证现场检查与药品质量标准、市场监督协同性的思考
9.GMP Attestation Accelerates Industrialized Upgradation of Veterinary Drug Enterprises of Shanxi;GMP认证加速山西兽药企业产业升级
10.How the Minor Pharmaceutical Enterprises to Finish GMP Certification;中小型制药企业如何完成GMP认证
11.Some View on GMP Inspection in Biological Products Manufacturers;生物制品GMP认证检查的几点体会
12.GMP certified plant/facilityGMP认证生产车间
13.On the GMP for Animal Drugs Certification Process in the Corporate Existence of the Problem and Recommendations;关于兽药GMP认证过程中企业存在的问题与建议
14.Continuous Study of Quality Improvement for Pharmaceutical Enterprises After Certification of GMP;GMP认证后制药企业质量改进的持续性研究
15.Risk-Resistant Function of OEM in GMP s Attestation of Biological Pharmacy Enterprises;OEM在生物制药企业GMP认证中的抗风险作用
16.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
17.Improvement and Optimization of Workshops, Facilities and Process Flow Design during the GMP Certification in Troche of Traditional Medicine对中药饮片GMP认证中厂房设施、工艺流程设计的改进及优化
18.Relationship Among Drug Marketing Authorization,Manufacturing Authorization as Well as GMP Inspection欧盟药品注册、企业生产许可证及GMP检查的相互关系

相关短句/例句

GMP compliance standard药品GMP认证检查评定标准
3)GMP authenticationGMP认证
1.It is important for a pharmaceutical enterprise to obtain GMP authentication.该文总结了企业通过GMP认证的体会是:应把GMP设计与GMP认证有机地结合起来;构建合乎GMP标准的软件体系;加强人员培训。
4)GMP certificationGMP认证
1.In order to complete GMP technical transformation and software construction within the period set by the state and pass smoothly through GMP certification.通过《药品生产质量管理规范》认证,是国家对制药企业必须施行的法规性要求,为在国家规定期限内完成GMP技术改造和软件建设,并顺利通过GMP认证,企业必须有一支精干的技术管理队伍,有对GMP较深刻理解的领导者,有一个清晰的工作思路,有一套行之有效的运行方法,就可以以较短时间、较少投入实现通过GMP认证的目标。
2.GMP certification system is not only a kind of methods supervising pharmaceutical enterprises in our country,but also scientific and advanced management to guarantee drugs quality.GMP认证制度是国家对药品生产企业监督检验的一种手段,也是保证药品质量的一种科学、先进的管理方法。
5)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。
6)Drug GMP management药品GMP管理