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 MoreAbout Us
Back in 1988, our CEO Mr. Gideon Elkayam founded Obelis: a small, family-run business with a grand vision to “create compliance for safer markets”.
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 MoreBREXIT WEBINAR: NEW UK guidelines explained

Recently the UK published its guidelines for the post-Brexit era, giving a NEW outlook of the long awaited UK regulations to be applied to medical device manufacturers wishing to place their medical devices on the UK Market after January 1st 2021.
In this webinar we covered:
- The UKCA Mark
- The expected UK requirements
- The differences between the UK and Northern Ireland
- The tasks and responsibilities of the UK Responsible Person
At the end of the webinar, we will also present a first look onto the UK RP services offered to medical device manufacturers by Obelis UK Ltd and as usual, we will make available special templates to support your compliance with the MDR.