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欧洲药典新章节草案“预混辅料”公布

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aiyao 发表于 2015-11-16 16:39:58 | 只看该作者 回帖奖励 |倒序浏览 |阅读模式

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20151111 ECA新闻:欧洲药典新章节草案“预混辅料”公布  
GMP News
11/11/2015
Draft of new Ph. Eur. Chapter"Co-Processed Excipients" published
欧洲药典新章节草案“预混辅料”公布
A draft of a new Ph. Eur. chapter "Co-Processed Excipients" has been published in Pharmeuropa 27.4 withdeadline for comments on December 31, 2015.
新的EP章节草案“预混辅料”在27.4中公布,征求意见截止日期为2015年12月31日。
In the proposed chapter aco-processed excipient is defined as "any combination of two or moreexcipients obtained by physical co-processing that does not lead to theformation of covalent bonds".
在拟定的章节中,预混辅料定义为“两种或更多种辅料通过物理预混获得的混合物,其中不含有分子键”。
The individual components of aco-processed excipient have to comply with the requirements of anycorresponding individual Ph. Eur monograph and of the general Ph. Eur.monograph Substances for pharmaceutical use.  Additionally,the co-processed excipients comply  with the requirements of the generalPh. Eur. monograph Substances for pharmaceutical use.
用于预混的单个辅料必须符合欧洲药典中相应的各论要求,以及药用物质的通论要求。另外,预混辅料还要符合药用物质通论的要求。
Co-processed excipients can be producedby processings that produce only a physical interaction between the componentslike for example co-drying, spray drying, granulation, extrusion, andhigh-shear dispersion. They may be batch or continuous processes.
预混辅料可以通过只会发生物理反应的工艺过程制得,例如,共同干燥,喷雾干燥,制粒,挤出和高剪切分散。这些工艺可以是间歇生产也可以是连续工艺。
The proposed monograph includes sectionson Characters, Identification, Tests, Assay, Labelling, andFunctionality-Related Characteristics.
所拟的各论包括部分为属性、鉴别、测试、含量、标签和功能性相关特性。
The section on "Tests"proposes that "specifications are defined for the final co-processedmaterial as a whole" and "if the co-processed excipient includesimpurities not controlled by the monographs of the individual components, thesemust be specified and suitably controlled".
在“测试”部分提议“为最终预混物料整体质量定义质量标准”,“如果预混辅料包括了单成分各论中未受控的杂质,则必须指明并进行适当控制”。
Following your registration on thePharmeuropa website you can get to the complete Draft Chapter "Co-Processed Excipients".
在欧洲药典网站注册后,你就可以获得完整的草案。

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