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

This article was originally published in SRA

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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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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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