GMP
美 
英
- n.一磷酸鸟苷；胞苷一磷酸；鸟苷酸；胞苷酸
- 网络药品生产质量管理规范(good manufacturing practice)；良好生产规范；良好操作规范
英汉解释
英英解释
例句
It may not be cost-effective to locate storage tanks as close as possible to the point of use, within high-cost, GMP -finished areas.
在高成本、区域内，尽可能靠近使用点安置贮水罐并不会节约成本。
The productive process is sealed and no dead corner, granulating uniform, easy to clean. It conforms to the requirements of GMP.
生产过程密闭无死角，制粒均匀、清洗方便，完全符合GMP要求。
It would be unrealistic to expect drug product GMP concepts to apply to the production of these progenitors.
使制剂的GMP概念适用于这些物质的生产是不现实的。
Create the GMP self-inspection plan of the company and participate in its implementation.
负责制定公司GMP自检计划，并参与组织实施。
The system of quality assurance incorporating GMP and quality control should be fully documented and its effectiveness monitored.
结合GMP和质量控制的质量保证系统应该完全文件化并有效监督。
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。
The designation of a device as a "custom" or "customized" device does not confer a GMP exemption.
以定制或定制化所指定的器械并不授予GMP豁免。
'This program makes you aware that there is more involved in GMP than you think. ' Jens de Jong, team leader Yamanouchi Pharma.
这套培训课件让你意识到，涉及到GMP的问题比你想象的还要多。
For instance, a molecule that mimics cyclic di-GMP could be used to disable or disarm bacterial infections such as cholera, he said.
他举例说，如类似环状二GMP小分子可以用失活或消除诸如霍乱这样的细菌感染。
For new projects, coordinate with related departments to follow up the GMP standard to revise and acceptance apparatus and instruments.
对新项目协调有关部门按照GMP标准对电器及仪表进行校正及验收；
Who in 60's of the last century began to develop drug GMP, China is from on 80 time begin the century implementation.
世界卫生组织上世纪60年代中末尾组织制定药品GMP，中国则从上世纪80年代末尾推行。
For the purposes of this guidance, the terms current good manufacturing practices and good manufacturing practices are equivalent.
本指南中的“现行优良生产管理规范（cGMP）”和“优良生产管理规范（GMP）”是等同的。
Train workshop staff to enable them to meet the GMP requirement in terms of hygiene, safety, quality and efficiency.
做好车间员工的培训工作，使其符合GMP车间岗位的卫生、安全、质量和效率要求。
This specification includes a general Good Manufacturing Checklist to be used as a tool by plant operations to evaluate GMP Compliance .
该标准包括一个全面产品制造检查表，生产厂管理层用它来评估GMP的符合性。
Why should GMP INSPECTION sometimes turn into a PAINFUL and CATACLYSMIC event ?
为什么GMP检查有时会成为一次痛苦的和非常大的事件？
SFDA will be on the site of the drugs production enterprise " GMP inspection certificate" continue to be publicity.
SFDA将在网站上对药品生产企业《药品GMP证书》延续情况予以公示。
At least 2 year related experience on quality in chemical, food industry, GMP experience is preferred.
2年以上相关化工，食品行业质量工作经验，具有GMP（良好生产操作规范）经验者优先；
NO was shown to work by elevating the tissue levels of another signaling molecule known as cyclic GMP .
进一步的研究显示，一氧化氮是通过提升生物组织中的另一种讯号分子环鸟？磷酸的含量而产生作用。
But by the time GMP enterprise also scarred, at a time when many small enterprise debt Liangsanqianwan.
不过经过那次GMP的企业也是伤痕累累，事前许多小企业负债两三千万。
The new version of GMP is about to publish the information again appetizing appetite pharmaceutical enterprises.
新版GMP即将发布的信息又一次吊足了制药企业胃口。
More recently , however, cyclic GMP- independent pathways have been discovered which can account for certain biological actions of NO .
不过，近期的研究发现了一些由一氧化氮引起的生物反应，是与环鸟？磷酸无关的。
object: To solve the problem of the flux control set of unfitting GMP demand in large infusion filling machine for soft packaging.
目的：为解决现用的软包装大输液灌装机流量控制装置不符合GMP要求的问题，对软包装大输液灌装机进行改进。
In charge of development and management of the company's GMP system.
负责开发和管理的公司的GMP制度。
Ensure effective quality control system and its compliance with GMP, internal requirements and the requirement of customers.
贯彻、执行有效的质量管理体系，确保质量管理体系与GMP及客户要求保持一致；
Inspection group generally does not exceed 3, check the members shall be the State Drug Administration drug GMP inspector.
检查组一般不超过3人，检查组成员须是国家药品监督管理局药品GMP检查员。
Make & implement sectional training plans. Continuously improve their technical skills, GMP awareness and professional skills.
建立并实施部门员工培训计划。持续改进其技术技能、GMP知识及专业技能。
responsible for the checking and qualifying of the equipment maintain, process and materials change that comply with sop and gmp.
负责检查和确保设备的维护、生产工艺和物料变更符合sop和gmp的相关要求；
At the moment, the production line for TCM products has been passed for GMP certification since 2005. IV. Project Brief: a.
目前，投入生产中药系列产品生产线已于2005年通过GMP认证。
This GMP Guide does not apply to steps prior to the introduction of the defined "API Starting Material" .
本GMP指南并不适用于确定的“API起始物料”引入前的步骤。
A full general GMP inspection is carried out in each year. In addition, inspections for parts of GMP system will be carried out every month.
每年执行一次全面的GMP检查，另外，每个月执行一次GMP系统的部分检查。
Draft and update GMP documents related with new product development; review manufacturing process documents of new products.
编写和修订与新产品开发相关的GMP文件，审核新产品的生产工艺规程。
Singapore businessmen sole proprietors of enterprises, through the GMP authentication.
为新加坡商人独资经营的企业，以通过GMP认证。
Results and Conclusion If enterprises have set up effective GMP system, an approval form FDA inspection would be safely assured.
结果与结论企业如果建立了有效的GMP制度，那么企业完全能够通过FDA的认证。
This Standard covers all physical , chemical , biological and microbiological GMP testing performed by Company Sites and Affiliates .
所有处理水的测试结果（化学和微生物）总体来说在标准范围内。
Pre-treated fresh air is supplied to controlled areas via a terminal HEPA unit mounted on the ceiling of each GMP cleanroom.
通过安装在各个GMP洁净室天花板上的终端HEPA装置（高效微粒空气过滤器）向受控区域提供预先处理过的新鲜空气。
Quality assurance department administers every aspect of medical production process, making sure all products conform with GMP standards.
质量保证部门全过程监督和管理药品生产，严格按照GMP要求规范生产。
Other additional responsibilities assigned by QA Manager. Support internal and external GMP & government inspection.
QA经理指定的其它工作。支持内部及外部GMP及政府部门检查。
Methods: The quality management were strengthened through three measures: quality standard, drug approval number and GMP management.
方法：从中药饮片的质量标准、批准文号管理和GMP管理三方面来加强中药饮片的质量管理。
With regards to the GMP, this initial distributor is responsible for maintaining complaint files and general record keeping requirements.
相关于GMP，该一级经销商应负责建立投诉文档并负责保留通常记录的要求。
All staff undergo strict GMP knowledge, skills training in the pharmaceutical, continuing the work of innovative capacity.
全部人员经过严格的GMP知识、制药技能的培训，具有持续创新的工作能力。
