Medical device companies in the EU should take a note:the updated MIR (Manufacturer Incident Report) form version 7.3.1, published on 23 March 2026, becomes mandatory from 1 May 2026. This …
MDR 2026 Revision: New Expectations for Phthalates and CMR Substances – What Manufacturers Need to Know
As of 1 January 2026, an important update to the Regulation (EU) 2017/745 (MDR) reinforces how manufacturers must assess hazardous substances in medical devices—especially phthalates, CMR, and endocrine-disrupting substances.This is …