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MedTech Europe is driving the improvement of IMDRF Adverse Event Terminology

Posted on 04.04.2024

In March 2024, the International Medical Device Regulators Forum (IMDRF) published its Adverse Event Terminology update. Out of 79 new or changed codes, 49 were requested by MedTech Europe. Overall, MedTech Europe has submitted the largest number of change requests and continues to be the biggest contributor to the improvement of IMDRF Adverse Event Terminology.

For more information, please contact Vaida Jukneviciute, Manager In Vitro Diagnostics.