The Medical Device Regulation (MDR) has significantly transformed the way medical devices are regulated in the European Union, replacing the previous Medical Devices Directive (MDD). For medical device manufacturers, this shift presents a range of challenges, particularly when it comes to obtaining the CE Marking, a key requirement for https://zanemqvaf.wikiworldstock.com/1094599/navigating_the_challenges_of_mdr_ce_marking_a_guide_for_medical_device_manufacturers