gmp的例句大全

the format of gmp certificate shall be uniformly provided for by the drug regulatory department under the state council.

《药品生产质量管理规范》认证证书的格式由国务院药品监督管理部门统一规定。

objective: to provide references for the improvement of our country's current good manufacturing practice ( gmp).

前言：目的：为完善我国《药品生产质量管理规范》（GMP）提供参考。

this study explored the economy-law effects of the good manufacturing practice ( gmp) for drugs in china and presented the limitation of gmp as economic law.

文章从经济法的视角对我国近年来逐步推行的药品生产质量管理规范（GMP）认证制度进行评析，指出其本身具备的经济法性质，分析其作为一项经济法律手段所存在的问题。

study on the economy-law effects of the good manufacturing practice ( gmp) for drugs in china

对我国药品GMP认证的经济法思考

secondly, the enterprises engaged in drug manufacture and trade should be regulated by the good manufacturing practice ( gmp) and good selling practice ( gsp).

其次，参与药品生产和销售的企业应该受到GMP和GSP的监管。

the first quality concern of a biopharmaceutical product is its safety and efficacy. thus requires that the whole production procedures must comply with the requirements of good manufacturing practice ( gmp).

生物制药产品的质量首先是要安全有效，生产过程必须遵守药品生产质量管理规范GMP质量管理的要求。

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.

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.

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.

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.

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: 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.

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.

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.

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.

Responsible for ensuring GMP compliance in production department activities.

负责保证生产部分操纵的GMP实施.

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.

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.

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.

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.