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New EU Medtech Scrutiny Procedure Less Widely Applicable And Less Complex Than Expected

This article was originally published in SRA

Executive Summary

One of the greatest hurdles in the future EU Medical Device and IVD Regulations - the highly demanding scrutiny procedures for high-risk devices and IVDs - now looks less widely applicable than industry had expected. Amanda Maxwell spoke with MedTech Europe's John Brennan and Jesus Rueda to find out more

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