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Home » MedTech Europe Warns Class D Diagnostics Vulnerable Under EU IVDR
MedTech Europe Warns Class D Diagnostics Vulnerable Under EU IVDR
The EU’s implementation of the new In Vitro Medical Device Regulation (IVDR) “has ground to a halt in the wake of the COVID-19 outbreak,” MedTech Europe said, pressing the European Commission for help with the transition process for high-risk devices.
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