Metecon

At Metecon, we are passionate enablers for your medical devices and in vitro diagnostics.

Our mission is to ensure your successful and compliant market entry by transforming complex regulatory requirements into clear, actionable strategies. But we don’t just stop at strategy – we roll up our sleeves and actively support you in the full implementation of these strategies. Whether you are developing a new product, advancing an existing one, or exploring new markets, we stand by your side as a trusted partner.

Our hands-on approach means that we not only guide you through every phase of the product lifecycle but also take charge of the regulatory execution. This includes the preparation of necessary documentation, managing verification processes, and ensuring that all regulatory submissions are handled with precision.

Our goal is to lighten your load, allowing you to focus on what truly matters: your innovations.

Additionally, we serve as your reliable CH-REP and EC-REP, ensuring your presence and compliance in Switzerland and the EU, giving you peace of mind that all regulatory aspects are under expert management.