gmp是什么意思_gmp的含义及用法
GMP
[,di:em'pi:]
abbr. 药品生产质量管理规范(Good Manufacturing Practice)
【专业释义】
药品生产质量管理规范
【双语例句】
Also support for arbitrary precision numbers will be added (using GMP), as the CLR has no support for them.
同时，由于CLR并不支持任意精度的数字，因此还会增加这一功能(使用GMP)。
The world now has the means to rapidly diagno malaria and treat it effectively” said Dr Robert Newman, Director of the WHO Global Malaria Programme (GMP).
“当今世界掌握了快速诊断疟疾并对其进行有效治疗的方法，”世卫组织全球疟疾规划(GMP)主任RobertNewman博士表示。
The Mos Mabhid Stadium in Durban, designed by GMP Architekten, features an array of eco-worthy design features and it doesn’t hurt that it’s pretty amazing looking especially at night.
德班的摩西马布达体育馆由GMP建筑师事务所设计，突出了一系列具生态价值的设计特色，同时并不影响它极为神奇的外观尤其在夜晚。
The main requirements that should be established in GMP of UHT plant are discusd in this paper.
文章列举了超高温奶生产的GMP中的主要内容。
GMP aims to help countries with the correct policy and technical advice, so that they are better equipped to fully u available funds and achieve results.
全球疟疾规划旨在帮助国家制定正确政策和提供技术建议，从而使它们更好地做好准备，以充分利用可动用的资金和实现结果。
GMP's work will also build on integrated approaches to infectious dias to further strengthen health systems and build public health capacity for the longer term.
全球疟疾规划/世卫组织的工作还将借鉴对传染病采取的综合方针，以便较长期进一步加强卫生系统和建设公共卫生能力。
Nantong General Pharmaceutical Factory，state GMP approved, is a production ba 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。
In addition, patients with rhuematic AF had higher levels of D dimer and GMP 140 compared with nonrhuematic AF( P <0.05).
另外还发现D-二聚体和GMP-140水平在风心房颤与非风心房颤之间存在差异(P<0.05)。
To verify compliance with the principles of GMP for APIs, regular internal audits should be performed in accordance with an approved schedule.
为确证是否符合原料药GMP原则，应当按照批准的计划进行定期的内部审计。
We have a GMP certified extract factory to produce all kinds of herbal extract .
我们有一个工厂生产的GMP认证提取各种中草药提取物。
If manufacturers perform the activities as required by the QS regulation and as expounded in this manual, they should be prepared for a GMP inspection of their operations by an FDA investigator.
如果制造商按本手册所解释的QS法规的要求那样完成这些活动，他们应该说已经为FDA的检查者对其运作进行GMP检查做好了准备。
The specific measures and schedule for implementing the GMP shall be formulated by the drug regulatory department under the State Council.
《药品生产质量管理规范》的具体实施办法、实施步骤由国务院药品监督管理部门规定。
Hualan is the largest producer of vaccine in Asia with a state of the art facility that operates according to sFDA GMP and EU
guidelines.
华兰是与最先进的设施，国家在亚洲最大的疫苗生产商的操作根据国家药监局GMP和欧盟的指导方针。
All Natural Factors products are manufactured in accordance with the Government of Canada's Good Manufacturing Practices (GMP), among the highest standards in the world.
所有自然因素的产品的制造按照加拿大政府的良好制造规范(的GMP ) ，其中的最高标准在世界上。
Be familiar with GMP specification and domestic design criteria, construction and acceptance criteria.
熟悉GMP规范和国内设计规范，施工规范和验收规范。
Any proposals for GMP relevant changes should be drafted, reviewed, and approved by the appropriate organizational units and reviewed and approved by the quality unit(s).
与GMP有关的任何变更提案都应当由相应的部门进行拟定、审核和批准，并由质量部门审核和批准。
A range of GMP / HACCP training products designed for educating personnel employed in the food packaging industry are now available from the International Food Safety & Quality Network website.
为培训从事食品包装行业者设计的GMP /HACCP培训产品的范
围现在国际食品安全和质量网络的网址上可以获得。
A distributor who only adds a label bearing their name and address is exempt from the GMP requirements.
经销商，如果只将他们的名称和地址添加在标签上，可以豁免GMP要求。
Internal laboratories are inspected as part of the FDA GMP inspection of the member factories.
内部实验室是作为GMP成员工厂检查的一部分而接受FDA检查。
This method helps make the whole production process into digitalized management and control. A production management model can be t up incorporating with GMP in pharmaceutical enterpris.
该方法使企业对药品生产的全过程进行信息化的质量管理和控制，搭建了制药企业中结合GMP信息的生产管理模型。
Manufacture of medicinal gas should comply with the basic requirements of GMP, with applicable annexes, Pharmacopoeial standards and the following detailed guidelines.
医用气体的工业制造必须按GMP的基本要求及相应的附件、药典标准和下述具体的原则。
