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German Device Benefit Assessments And EU MDR In Industry's Sights

This article was originally published in SRA

Executive Summary

As the EU Medical Device Regulation limps towards the finish line, German industry association BVMed is keeping in its sight both the additional scrutiny for high-risk products that the MDR is likely to introduce and the medtech benefit assessment provision under Germany's Care Provision Strengthening Act (GKV-VSG).

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