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EU Regulation Medical Device

Heading For Crisis: The Upturn In EU Medtech Regulatory Output Is ‘Not Enough’ – MedTech Europe

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Executive Summary

There has been a flurry of EU Regulation implementation documents of late. The European Commission’s Rolling Plan is moving along, and there has been positive news of more notified body designation applications. But MedTech Europe still believes the sector is heading for a crisis  ̶  which member state authorities are aware of but won’t flag up, as Amanda Maxwell discovered in an exclusive interview with MTE’s Oliver Bisazza.

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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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