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MedTech Europe publishes a Call to Action on the MDR to keep devices available to patients

Posted on 06.02.2020

On 8 January, MedTech Europe published the document Implementation Status of the Medical Devices Regulation: a Call to Action. This document highlights the key remaining challenges to be addressed by the end of the MDR transition period, which need urgent solutions by EU policymakers in order for the industry to lawfully keep medical devices available to patients.