Welcome to your trusted partners in Switzerland

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Representation and support for manufacturers in the healthcare, beauty, and other industries.

Representative services

Since 1988, we create compliance for safer markets in the EU, Switzerland, and the UK.

About us

We support your products’ launch to the Swiss market through documentation review and product registration.

Registration services

Our services

Here’s what we do as your consultants & representatives for the Swiss market.

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We act ...

as your professional Swiss Authorized Representative.

We are ...

… certified according to ISO 9001: 2015 and ISO 13485: 2016.

We review ...

your medical devices’ technical documentation.

Why Obelis?

KOur deep knowledge of the Swiss, European and United Kingdom compliance frameworks make us the best choice to support your products’ path towards compliance in these territories. Our team is composed of dozens of regulatory experts that will guide you through medical devices’ technical documentation, notification, labeling, and much more. In addition, we are members of professional EAR Associations and Commission Working Groups.

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Our latest news

Swissmedic urges all manufacturers to review their PMS documentation

Swissmedic urges medical device manufacturers to review their post-market surveillance (PMS) documentation after finding major non-conformities in recent assessments. Learn more about compliance with MedDO requirements

EU and Swiss alignments: legacy devices and beyond

Switzerland aligns its IVD regulations with the EU from 1 January 2025, extending compliance deadlines and simplifying labelling to ensure supply chain stability and strengthen EU-Swiss collaboration.

Woman holding shopping basket with cosmetic products.

How to sell cosmetics in Switzerland: Regulatory considerations for brand owners

Comprehensive guide on selling cosmetics in Switzerland, detailing key regulatory considerations for brand owners.