EU Representation
Representing non-EU based manufacturers in a successful EU Market entry and safeguarding their future across the entire community.
Learn MoreEU Product Registration
Ensuring compliance and registering products to be made available on the EU Market.
Learn MoreTechnical Documentation Review & EU Submissions
For your products to legally enter the EU Market and continue to circulate, you must have valid documentation.
Learn MoreEU Consultancy, Legal & Training
Find your way through a complicated EU marketplace with the support of a professional.
Learn MoreCareers at Obelis
Take the first step to a consulting career that helps build a safer Europe.
Learn MoreTestimonials
We have provided compliance and consulting services for more than 3000 manufacturers in over 60 countries, helping them successfully introduce products to the European market.
Learn MoreContact Us
Our head office is in Brussels and we have a network of offices in 11 different countries including the US and Israel.
Learn MoreInternational Representatives
An experienced EU compliance representative is just a call or meeting away…
Learn MoreObelis International Offices (OIO) Network
Obelis International Offices are independent partners who are able to provide our clients with solutions in other global markets of their choosing.
Learn MoreMDR DELAY: WHAT HAS CHANGED?

Remember, the 1-year delay will provide you with additional time to finalize your compliance with the MDR, which is a complex and lengthy process!
But what does this entail for Medical Device manufacturers?
Join the FREE MDR Webinar to find out and hear the latest changes from the regulatory experts! We will be covering:
- MDR delay explained
- Vigilance & Incident Reporting after DoA
- Update a Clinical Evaluation Report based on the MDR