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首页> 外文期刊>International Journal of Pharmaceutical Sciences Review and Research >A Comparative Study: Good Manufacturing Practice (GMP) Requirements for Herbal Products: India & Europe
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A Comparative Study: Good Manufacturing Practice (GMP) Requirements for Herbal Products: India & Europe

机译:比较研究:草药产品的良好生产规范(GMP)要求:印度和欧洲

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The Present study deals with a brief overview of the GMP requirements for herbal products manufactured in India & Europe. Herbal medicine have always played an important role in the primary health care therefore should be manufactured under Good Manufacturing Practice (GMP) to ensure the quality & safety of the finished product. It is necessary to know the differences in the requirements of guidelines given by India & Europe. These guidelines focus on general requirements for quality assurance & quality control in manufacturing of herbal medicinal products. These guidelines will promote & improve the quality of herbal medicines & reduce the poor quality of herbal medicines. When these guidelines were compared, certain similarities & differences were observed.
机译:本研究简要概述了印度和欧洲制造的草药产品的GMP要求。草药在初级保健中一直起着重要作用,因此应按照良好生产规范(GMP)生产,以确保成品的质量和安全性。有必要了解印度和欧洲给出的准则要求之间的差异。这些准则侧重于草药产品制造中质量保证和质量控制的一般要求。这些准则将促进和改善草药的质量,并减少草药的劣质。当比较这些指南时,观察到某些相似和不同之处。

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