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EUSwissMed

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As a European Authorized Representative (EAR) with regulatory expertise in medical device technology and IVD EUSWISSMED sets new standards. As an entrepreneurial, solution-oriented partner for all aspects of the MDR and IVDR, we support our customers in implementing European requirements in German, English and French in a reliable and targeted oriented manner addressing the needs of medium-sized companies: From the creation / optimization of the Technical Documentation, product registration work with EUDAMED to support in market surveillance activities. EUSWISSMED – your reliable partner in the demanding healthcare market.

Company’s Keywords:

authorized representative, mdr, ivdr, technical documentation

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