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Isra Jofi
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EU Representative for MDR 2017/745 and IVDR 2017/746

According to EU MDR, 2017/745 and IVDR 2017/746, an European Authorized Representative is mandatory for Non EU manufacturers wishing to sell medical devices

Visit for more information - https://www.i3cglobal.com/eu-representative/

European Authorized Representative | EU Rep Services

According to EU MDR, 2017/745 and IVDR 2017/746, an European Authorized Representative is mandatory for Non EU manufacturers wishing to sell medical devices
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