To register a medical- or in-vitro diagnostic device in the European (EU) market can be easy with an experienced partner and informed authorised representative by your side. We are legal & regulatory experts and have a profund knowledge of the requirements that need to be fulfilled, if you decide to sell your medical device in one of the largest economies in the world.

To provide you with the best support our team is growing – but at the moment these are your experts @ qtec EuRep GmbH: