Medical device testing for EMC/radio compliance – Requirements of MDR and RED

The Medical Device Regulation (MDR) includes General Safety & Performance Requirements (GSPR) for active devices such as electromagnetic compatibility (EMC) requirements. As medical devices become increasingly complex, many manufacturers are now using radio technologies such as Bluetooth, WLAN or RFID. Medical devices with integrated radio technologies also fall under the scope of the Radio Equipment Directive (RED) 2014/53/EU, which also includes essential requirements.

How to address the new obligations introduced by the Radio Equipment Directive (RED)? How to handle special environments of your medical devices and specific risks associated with radio equipment in close proximity to medical devices? This webinar will provide an overview of the overlapping areas of MDR and RED requirements in the field of EMC, as well as practical solutions on how to proceed with already certified or uncertified radio modules. The webinar will also address the latest developments in medical EMC standardisation (e. g. IEC 60601-1-2).

Date and time: Tuesday, 3 November 2020, 7:30 pm (CET)

Your speaker: Hannes Adelsberger, Group Manager EMC


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