Current Edition

The MDR: The Clock is Ticking

The European Union (EU) Medical Device Regulation (MDR) is the biggest challenge to the medical device industry in over 20 years. With the new regulations come more stringent requirements, which must be met for the product to obtain a CE mark and be commercially available in the EU. Dr. Sergio Perez at Kolabtree shares insight into the MDR and what it means for medical device manufacturers.