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Medworld器械世界为您提供准确、及时、有效的医疗器械行业及医疗圈的市场动态,产品信息,技术进展等资讯。 来源 :MDDI Complex approval processes and high cost are among the challenges causing US medical device manufacturers to question whether the European Union Medical Device Regulations (EU MDR) are worth the time, effort, and expense. To put the pros and cons into perspective and offer potential solutions for US manufacturers who choose to remain in the potentially less crowded EU marketplace, Leeanne Baker, managing director and senior quality assurance and regulatory affairs consultant at IMed Consultancy, will lead the Should I Stay or Should I Go? The Silver Lining of Sticking Around After EU MDR panel discussion at Advanced Manufacturing Minneapolis (MD ), October 16 and 17. The numbers More than eight in 10 companies say the time it takes to secure permits is a barrier to investing in Europe, according to a BusinessEurope
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