It's time for a change at the helm of the EU authority group that works on MDR/IVDR implementation planning to help prioritize much-needed documents and actions to ensure the new EU regulatory system is working as effectively as possible.
Thomas W Møller, section manager of medical devices in the Danish Medicines Agency, has been elected chair of the executive board of the EU’s CAMD (Competent Authorities for Medical Devices) network.
CAMD is an umbrella group, under which the European national competent authorities work to enhance their level of collaborative work...
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