Join the U.S. Commercial Service for a focused webinar on navigating the complexities of the European Union’s medical technology market. The EU continues to be one of the world’s most advanced and opportunity-rich regions for med tech innovation, but the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) frameworks present significant challenges for U.S. exporters.
This session provides clear insights into regulatory requirements and commercial opportunities in Germany and Italy, two of Europe’s most dynamic med tech ecosystems. The content is tailored for exporters seeking a deeper understanding of EU market pathways and strategic opportunities in 2026 and beyond.