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&lt;/script&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://www.medq.eu/mdr-european-authorized-representative-services/embed/" width="600" height="338" title="&#x201C;MDR European Authorized Representative Services&#x201D; &#x2014; MedQ Consultants" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;</html><description>Heerlen, 27 October 2020 &nbsp; MedQ Consultants B.V. will continue to provide EU Authorized Representative services under the Medical Device Regulation (EU) 2017/745 (MDR). When the MDR was released, it became clear that the regulation adds more stringent obligations to manufacturers and authorized representatives. The obligations of authorized representatives are described in MDR Article 11. [&hellip;]</description></oembed>
