近年来,我国医疗器械出口持续增加,国产医疗器械迎来前所未有的发展机遇,但也面临境外法规差异及产品认证难的挑战。
为助力本土医疗器械企业抢抓欧盟市场出海机遇,精准破解欧盟MDR合规、临床评价、质量管理体系、网络安全、生物学及CMR合规等出海欧盟合规痛点:
杭州市市场监管局特邀请欧盟医疗器械MDR合规及认证专业机构定于2026年6月12日在杭州举办第一期医疗器械出海欧盟MDR专场公益培训。
Applus+ Laboratories再度携手瑞旭集团,联合推出本期医疗器械出海公益培训研讨会。
届时,我们将邀请CE MDR公告机构审核员、国家注册QMS/EMS/OHSMS管理体系审核员,以及资深医疗事业部营销总监亲临现场,为企业带来最前沿的专业解读。
作为全球领先的检测、检验、认证机构,Applus+ Laboratories在医疗器械领域深耕多年,不仅是欧盟MDR双公告机构(NB 2764 & NB 3121),更拥有覆盖全球的测试网络,致力于为企业提供一站式出海解决方案。
时间:2026年6月12日(星期五)
地点:杭州市临平区东湖街道五洲路17号1号楼4楼会议室(杭州微策生物西门进)
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