- Forrás: fda.gov news, 12 February 2026
Device Delivers Non-invasive Therapy and Supports Care at Home

Experts from the European Commission shed light on the proposed wide-ranging changes to the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) that have been put forth to the European Council and European Parliament for adoption. They say the changes are intended to address shortcomings in the legislation that have significantly delayed their full adoption over the past few years.