The European Union is one of the world’s largest and most highly regulated medical device markets, serving over 500 million consumers and generating more than €150 billion annually.

Achieving MDR or IVDR compliance is essential — but it’s only the first step. To legally place your device on the EU market, you must appoint a qualified EU-based Local Representative.

At CMS SciDoc, we deliver reliable, fully compliant, and responsive EU Local Representative services tailored to:
💠 Medical Devices (MDR 2017/745)
💠In Vitro Diagnostics (IVDR 2017/746)
💠Software as a Medical Device (SaMD)
💠Startups and Global Manufacturers

With over 33% of global medtech revenue generated in Europe, the opportunity is significant. Our expertise ensures not only regulatory compliance but also a smoother pathway to market success.

Partner with confidence. Expand with certainty.

Book your FREE consultation today and take the next step toward accessing the European market.
📩 info@cmsscidoc.com