Suppr超能文献

欧洲儿科监管框架实施六年进展回顾。

Progress review of the European Paediatric Regulatory Framework after six years of implementation.

机构信息

Paul-Ehrlich-Institut, Bundesinstitut für Impfstoffe und biomedizinische Arzneimittel, Federal Institute for Vaccines and Biomedicines, Paul-Ehrlich-Str. 51-59, 1 63225 Langen, Germany.

出版信息

Int J Pharm. 2014 Aug 5;469(2):240-3. doi: 10.1016/j.ijpharm.2014.03.019. Epub 2014 Mar 6.

Abstract

The EU regulation (EU 1901/2006 Paediatric Regulation) that entered into force in 2007 has changed the field of medicinal drug development for children in the EU. Five years after its implementation a large number changes due to this regulation have been incorporated by Pharmaceutical Industry considering the development of new candidate drug. This report is a review of changes already implemented and the aspects of paediatric drug development, which still needs to be addressed in future working in the fields to provide better medicines for children.

摘要

欧盟法规(欧盟 1901/2006 年儿科法规)于 2007 年生效,改变了欧盟儿童药物开发领域的格局。该法规实施五年后,制药行业在开发新候选药物时考虑到大量变化,已经对其进行了整合。本报告回顾了已经实施的变化以及儿科药物开发的各个方面,这些方面仍需要在未来的工作中加以解决,以为儿童提供更好的药物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验