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Experience the possibilities to bring you Medical Devices and In Vitro Diagnostics on the Swiss market. As your Swiss Authorized Representative, MedNet EC-REP assists you with all regulatory needs to ensure a quick and uncomplicated market access.
Medical Devices on the Swiss market are regulated by the MedDO. This regulation requires non-Swiss manufacturers to appoint a Swiss Authorized Representative (CH-REP) and to register their Medical Devices with the local authority Swissmedic. MedNet as your CH-REP will guide you through the Swiss regulatory landscape. Additionally we support you with quick and uncomplicated services for a short time to the market.
DetailsTo access the Swiss market and to register products in the field of In Vitro Diagnostics non-Swiss manufacturers must appoint a Swiss Authorized Representative to register their product with the local authority Swissmedic. MedNet, as your CH-REP, leads you through the requirements of the Swiss regulations and provides you with quick and uncomplicated services for your IVDs.
With our experts situated in Great Britain, we offer the necessary services for your products. With over 25 years of experience and an interdisciplinary team, we possess a profound understanding of the relevant regulations to provide you with comprehensive support.
We carry out fast and straightforward registrations in all EU member states, as well as in Great Britain and Switzerland.
We offer full service and a fast turn around for Free Sales Certificates. Including legalizations for almost every Country in the world if required.
Place all your regulatory needs into our hand:
Our intercultural team of PhD biologists and Medical Engineers will take care of your concerns - with one single point of contact and no matter which country you want to distribute into next.
