1、

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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2、

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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3、

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.

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4、

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.

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5、

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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6、

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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7、

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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8、

Operated at sealed negative pressure and designed by GMP.

密封负压操作,按gmp规范设计.

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9、

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.

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10、

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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11、

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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12、

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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13、

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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14、

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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15、

Familiar with GMP requirement is preferred.

熟悉药品生产GMP的要求者为佳.

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16、

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。

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17、

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。

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18、

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

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19、

GMP Construction of Axenic Workshop of Animal Powdery Agent

兽药无菌粉针车间的GMP建设

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20、

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。

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