We are French consultants with several years of experience in the field of medical device regulation.

We have encountered the same challenges as almost all regulatory experts during the implementation of the EU MDR 2017/745 and EU IVDR 2017/746.

After several years of expertise in implementing these regulations, we decided to share our knowledge and experience to make the regulations accessible to everyone!

Therefore, we created EU MDR COMPLIANCE, which is nothing less than a group of enthusiasts who love regulation (yes, it's possible). But what we love most is sharing, exchanging, and responding precisely to your needs because ultimately, we encounter the same issues!

We share regular content on LinkedIn; you probably met us through this platform!

"It's because we have managed to solve the same problems that every regulatory expert encounters that today we share our knowledge and expertise."