European Legislation and Research Projects regarding Patient Education for Medication

R. Vander Stichele, Marc G. Vander Bogaert
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引用次数: 2

Abstract

In 1992 the European Community adopted Directive 92/27/EEC “On the labeling of medicinal products for human use and on package leaflets,’’ implementing the mandatory inclusion of full in formation leaflets written in understandable language in every medication package between January I , 1994 and December 31,1998. This article describes the features and historical motives of this new legislation. In addition, it reviews European research projects on the impact of written medication in formation.
关于患者用药教育的欧洲立法和研究项目
1992年,欧共体通过了第92/27/EEC号指令“关于人用药品的标签和包装说明书”,强制要求在1994年1月1日至1998年12月31日期间,在每个药品包装中都必须包含以可理解语言编写的完整信息说明书。本文描述了这一新立法的特点和历史动机。此外,它还审查了欧洲关于书面药物信息影响的研究项目。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Information Journal
Drug Information Journal 医学-卫生保健
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6-12 weeks
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