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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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Familiar with GMP requirement is preferred.

熟悉药品生产GMP的要求者为佳.

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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.

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To file the batch record in the GMP library termly.

将批记录定期归档在GMP图书馆.

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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.

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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.

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The optimum structure is adopted according to GMP requirements.

该机采用了适合GMP要求的优化结构.

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Responsible for ensuring GMP compliance in production department activities.

负责保证生产部分操纵的GMP实施.

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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.

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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.

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