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[欧盟传统草药产品法律法规难点问题分析]

[Analysis of difficult problems on European Union laws and regulations of traditional herbal medicinal products].

作者信息

Qu Li-Ping, Zhang Xiao-Qun, Xiong Yan, Wang Yi-Tao, Zou Wen-Jun

机构信息

College of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 610041, China.

Institute of Chinese Medical Sciences, University of Macau, Macau 999078, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2017 Oct;42(20):4040-4044. doi: 10.19540/j.cnki.cjcmm.20170913.002.

Abstract

Registration of Chinese patent medicine in European Union (EU) is of great significance to the internationalization of traditional Chinese medicine as EU market acts as an important position in the global botanical market. In retrospect, the domestic studies on EU regulations of traditional herbal medicinal products have been conducted for more than 10 years, but there is still some cognitive bias and lack of research. In this paper, a review of the relevant research progress and the main misunderstanding problems about Directive 2004/24/EC, like the centralized and decentralized supervision system of traditional herbal medicinal products in the EU, marketing authorization procedures for traditional herbal medicinal products, Community Herbal Monograph and List Entries, would be systematically analyzed, so as to provide reference for the registration of Chinese patent medicine in EU.

摘要

中成药在欧盟注册对中医药国际化具有重要意义,因为欧盟市场在全球植物药市场中占据重要地位。回顾过去,国内对欧盟传统草药产品法规的研究已开展了十多年,但仍存在一些认知偏差和研究不足。本文将系统分析有关欧盟传统草药产品集中和分散监管体系、传统草药产品上市许可程序、《欧盟草药专论》及列入清单条目等方面关于2004/24/EC指令的相关研究进展及主要误解问题,为中成药在欧盟注册提供参考。

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