GMP的例句大全

All numbering within this section coincides with actual numbering in the GMP Provision.

本节中的所有编号与GMP规定的实际编号一致.

The standardized management of GMP document administrate the production process in pharmaceutical enterprises in standardization.

本文从制药企业工作中的实际问题出发,探讨企业在GMP文件管理中的常见问题和解决方法.

Ensure Production batch record are properly completed according to GMP documentation requirements.

按照GMP记录的要求,制作并完成批生产记录.

Implement sectional training. Continuously improve their technical skills, GMP awareness and professional skills.

实施部门员工培训. 持续改进其技术技能 、 GMP知识及专业技能.

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.

Objective: For availably control the clean room's airborne, the clean room's cleanliness attaining the GMP rulinging.

目的: 为了有效地控制洁净室的尘埃粒子数, 使洁净室的洁净度达到GMP规定的要求.

Laboratory, clean room, control room, datarooom, hospital, GMP drug factory , food factory , electronic factory, textile factory.

实验室 、 无尘(菌)室 、 仪控室 、 资料室 、 医院 、 GMP、药厂 、 食品工厂 、 电子 、 纺织厂等.

OBJECTIVE : To provide approaches and avenues for the Chinese drugs preparations manufacturers in the GMP depuratory authentication.

目的为中药制剂生产机构的GMP清洁验证工作提供方法和思路.

Responsible for other GSP relevant issues in trading function and GMP execution matters in Development lab.

负责贸易公司其他GSP事宜和在小试车间的GMP实施情况.

GC 8901 in terms of GMP and HMW-GS contents, flour sedimentation value, farinograph parameters and extensograph parameters.

藁城8901籽粒谷蛋白、GMP含量、HMW-GS含量 、 面粉沉淀值 、 粉质仪参数和拉伸仪参数显著高于山农1391.

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.

Familiar with GMP requirement is preferred.

熟悉药品生产GMP的要求者为佳.

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.

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.

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.