Opportunities and impacts of the new MDR regulations.
The new MDR regulations have a major impact on many European companies. As of May 26, 2021, all medical devices sold to the EU will have to be certified
and registered. Although this means a lot of extra time and financial effort for all parties involved, it is an important step forward and valuable for the AT market. The regulations raise awareness and lay the foundation - the AT industry hopes - for continued excellent services and improved product quality. Various opinions and insights from manufacturers, importers, retailers and MDR experts provided plenty of material for a lively industry exchange at the 3rd ATF-Talk.
Participants in the panel discussion: Nadine Farris (Inclusive Technology Ltd.), Jürgen Kohl (Rehavista), Paul Thompson (Ablenet), Jeff McBride (Alveo Technologies), Paul Rowden (European Device Solutions Ltd.) and Fiore Capone (Active Communication).
More than 70 participants followed the online meeting.