One of the most surprising – and positive – pieces of EU regulatory news in April was that fully 47 notified bodies have now applied to the European Commission to be designated under the new Medical Device and IVD Regulations. (Also see "Sharp Rise In EU MDR Notified Body Applicants Is Pleasant Surprise" - Medtech Insight, 24 April, 2019.)
What is more, almost all the applications are to audit products under the full scope
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