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Authorized EU Representative for Design Dossier and Free Sale Certificate at Qualimedtech

Design Dossier for Medical Device requires implementation of the quality management system.

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Authorized EU Representative for Design Dossier and Free Sale Certificate at Qualimedtech

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  1. Authorized EU Representative for Design Dossier and Free Sale Certificate at Qualimedtech If you are looking to sell medical device then you must understand US FDA medical device registration. Design Dossier for Medical Device requires implementation of the quality management system. Qualimedtech can provide full range of the service to their clients such as establishment registration, medical device listing, document preparation, US FDA submission through European Representative CE Marking US agent and solving technical queries. This particular company actually serves EU regulations and EU Representative Fees information for all medical device manufacturers and also importers all over the world. This QualiMEDtech Company helps you Technical File CE Marking with filing for your medical device with all relevant details about your device to outline the performance, efficiency and also its safety. For more information about our services, visit our website: http://www.qualimedtech.de Our Contact Address: Bremen, Germany - 28207 Tel: +49 42187826105 Email: info@qualimedtech.de Liberty Management Group LTD Aurora, Illinois, USA - 60504 Phone: +1 6302702921 I 3 Consulting Bangalore, Karnataka, India - 560029 Mobile / WhatsApp: +91 9945912081

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