GMP的例句大全

Perform all activities in compliance with relevant GMP and Quality Systems standards.

在相关的GMP和质量体系标准的要求下履行职责.

A pilot plant complies with GMP has been established for trial production.

建立了符合GMP的中试车间用于新产品试产.

Familiar with quality system requirements of GMP, ISO, FDA and related regulatory.

熟悉GMP 、 ISO 、 FDA与相关法规的质量管理体系要求.

Responsible for renewing of production license, GMP certificate etc. according to regulations.

负责根据法规更新生产许可证, GMP证书等.

Carry out GMP and Safety regulation in process equipment maintenance.

在工艺设备维护工作中,贯彻执行安全和GMP法规.

Result: validation is the base of GMP in medicine producing.

结果: 说明验证是药品生产中GMP的基石.

To file the batch record in the GMP library termly.

将批记录定期归档在GMP图书馆.

Operated at sealed negative pressure and designed by GMP.

密封负压操作,按gmp规范设计.

Features: accurate liquid level, easy to operate, accorded with GMP.

特性: 液位准确 、 操作方便, 符合GMP要 示.

Continuously improve their technical skills, GMP awareness and professional skills.

持续改进其技术技能 、 GMP知识及专业技能.

Experience from pharmaceutical quality control laboratories and knowledge of GMP is desirable.

要有制药行业质量控制实验室工作经验,以及GMP知识.

The optimum structure is adopted according to GMP requirements.

该机采用了适合GMP要求的优化结构.

Responsible for ensuring GMP compliance in production department activities.

负责保证生产部分操纵的GMP实施.

Understanding of the ISO 9000 and GMP system and have some practice experience.

了解ISO9000和GMP管理体系,并具有一定的实务操作经验.

Familiar with GMP requirement is preferred.

熟悉药品生产GMP的要求者为佳.

PD-type centrifuges are a new type, designed and manufactured according to the standard of pharmacy equipment GMP.

PD型离心机是依照制药装备GMP规范设计制作的新机型。

Cyclic AMP ( cAMP) and cyclic GMP ( cGMP) are of pivotal importance in determining many aspects of cellular function.

环腺苷酸（cAMP）和环鸟苷酸（cGMP）对于细胞的许多功能有重要作用。

NMR studies on the conformation of cyclic AMP and cyclic GMP in solution

环状AMP和GMP环状溶液构象核磁共振研究

GMP Construction of Axenic Workshop of Animal Powdery Agent

兽药无菌粉针车间的GMP建设

Based on GMP norm, the requirements for the equipment used in axenic raw drug production were discussed in this article.

依据GMP规范，对无菌原料药生产过程中设备的要求进行讨论。