The Role of New Technology in Post-Market Surveillance of Medical Devices
Technology
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The Role of New Technology in Post-Market Surveillance of Medical Devices

December 14, 2022
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The European Medical Device Regulation (EU MDR) is excessively replacing the regulatory framework for medical devices. One of the new significant challenges is the increased focus on clinical proof and Post-Market Surveillance (PMS). A recent article published by Emergo by UL warns that medical device companies will have to place

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