Motor Vehicles

Non-European manufacturers are strongly encouraged to appoint a professional European Authorised Representative. This allows to stay informed about necessary documentation, applicable standards, or ongoing changes in the applicable requirements relating to the product.

Obelis, located within walking distance of the European Commission, acts as your Authorised Representative in Europe and Switzerland and as Responsible Person in the United Kingdom.

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Compliance Success Stories

Why Obelis?

Our deep and long-standing experience with Swiss, EU and UK compliance frameworks makes us the best choice to support your products’ path towards compliance in these territories.

Our team regulatory experts will guide you through medical devices’ technical documentation, notification, labelling, among others.

About us
Founded in 1988, we are among Europe’s largest centres for advisory and representative services.
We are certified by ISO 9001:2015 and ISO 13485:2016.
We have helped over 3,000 manufacturers from over 60 countries address their regulatory challenges.
We are members of professional associations and more than 10 European Commission working groups.
Obelis International Offices (OIO) comprise independent partners providing solutions in other global markets.
Our team consists of lawyers, chemists, pharmacists, and other experts. Our close-knit culture has been certified by the Great Place to Work Survey 2022-23.