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Guido Rasi: a day in the life of the European Medicines Agency's executive director

机译:吉多·拉西(Guido Rasi):欧洲药品管理局执行董事的一天

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My interview with European Medicines Agency executive director Guido Rasi gets off to an ominous start.An urgent matter has cropped up and Professor Rasi is now running late after having to deal with a morning of unscheduled meetings.It is 26 October and France has just announced it is suspending sales of Novartis's Agrippal flu vaccine as a precautionary measure, after potential quality defects were found in batches of the drug.The EMA is busy preparing a statement on the matter; the agency's head of communications informs me. I half expect my interview to be cancelled but Prof Rasi manages to squeeze me into his increasingly hectic day.Prof Rasi took over the helm of the EMA in November 201 I. Since then, as well as dealing with the typical responsibilities entailed in running an agency that regulates medicines for over 500 million citizens in the EU, he has been busy with the colossal job of implementing the new pharmacovigilance legislation
机译:我对欧洲药品管理局执行主任吉多·拉西(Guido Rasi)的采访开始了一个不祥的开始,紧迫的事情已经解决,拉西(Rasi)教授在处理了一场不定期的会议之后,现在已经迟到了.10月26日,法国刚刚宣布作为预防措施,在一批药品中发现潜在的质量缺陷后,该公司正暂停诺华的Agrippal流感疫苗销售。EMA正在忙于准备此事的声明。该机构的沟通负责人通知我。我一半希望我的面试被取消,但Rasi教授设法将我挤进了他日趋忙碌的一天。Rasi教授于201 I年11月接管了EMA的职务。从那时起,他开始处理与执行EMA有关的典型职责。负责监管欧盟超过5亿公民药品的机构,他一直忙于执行新的药物警戒法规的艰巨工作

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