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Webinar
眼镜产品进入欧洲(欧盟/英国)市场 准入标准网络研讨会
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DATE
Aired On
30 Jul 2021 |
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TIME
On-Demand
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FEE
免费
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LANGUAGE
Chinese
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TOPIC
Lab Testing
Bodycare, Fashion & Accessories
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SPEAKER
Davio Tsang
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ORGANIZER
events@qima.com
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欧盟委员会、议会和理事会等机构为应对医疗器械不断变化的需求,于2017年4月5日对医疗器械法规进行全面修订,并发布了新的医疗器械法规MDR(EU)2017/ 745。新法规取代了 MDD 93/42/EEC,并已于2021 年5 月 26 日实施生效。
这意味着欧盟成员国对医疗器械产品将发生重要变化,为此,本次研讨会将邀请启迈QIMA专家Davio为大家讲解当下眼镜产品进入欧盟及英国市场的最新标准。
时间:2021年7月30日14:30
语言:普通话
费用:免费
报名后,将于会议开始前一天发送直播间链接及提醒,请留意。
Davio Tsang为启迈QIMA眼镜行业技术专家,拥有眼镜制造业超过10年的经验。后加入检测服务业长达10年,检测对象为包括国内主要生产眼镜的厂家及欧美等地区的买家、眼镜连锁店及分销商。Davio 曾在HKOMA香港眼镜厂商会及海外等多次演讲关于眼镜测试标准及规定。
QIMA is a leading provider of supply chain compliance solutions, that partners with brands, retailers and importers to secure, manage and optimize their global supply network.
QIMA has on-the-ground presence in 95 countries, combining industry-leading experts for onsite inspections, supplier audits and lab testing with a digital platform that brings accuracy, transparency and intelligence for quality and compliance data.
For all our clients in 120 countries who use the QIMA platform and benefit from 24/7 support in over 20 languages, QIMA is Your Eyes in the Supply Chaintm.
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