1)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。
英文短句/例句
1.GMP certified plant/facilityGMP认证生产车间
2.Validation of Autoclaves for GMP CertificationGMP认证中对高压蒸汽灭菌器的验证
3.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
4.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
5.Discussion of GMP Certification in Pharmaceutical Enterprise after 2004 in China;关于2004年后我国GMP认证工作的探讨
6.Some View on GMP Inspection in Biological Products Manufacturers;生物制品GMP认证检查的几点体会
7.How the Minor Pharmaceutical Enterprises to Finish GMP Certification;中小型制药企业如何完成GMP认证
8.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
9.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
10.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
11.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
12.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
13.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
14.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
15.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
16.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
17.Nantong General Pharmaceutical Factory， state GMP approved, is a production base for active pharmaceutical ingredients and intermediates.南通制药总厂是获准国家GMP认证的化学合成原料药及医药化工中间体生产基地。
18.Pay Close Attention to the Anew Authentication of Drugs GMP重视和做好药品GMP重新认证工作
相关短句/例句
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。
3)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。
4)GMP verificationGMP验证
5)GMP compliance standard药品GMP认证检查评定标准
6)GMP Quality AssuranceGMP质量保证体系
延伸阅读
GMP认证 GMP是英文GoodManufacturingPractice的缩写，中文的意思是“良好作业规范”，或是“优良制造标准”，是一种特别注重制造过程中产品质量与卫生安全的自主性管理制度。它是一套适用于制药、食品等行业的强制性标准，要求企业从原料、人员、设施设备、生产过程、包装运输、质量控制等方面按国家有关法规达到卫生质量要求，形成一套可操作的作业规范，帮助企业改善卫生环境，及时发现生产过程中存在的问题并加以改善。产品质量环境标准管理标准
