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Medical Device

EMA invites comments on consultation process for drug/device products

This article was originally published in Clinica

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Executive Summary

The European Medicines Agency has launched for comment a 16-page draft guidance on how notified bodies consult the agency on products that combine devices with "an ancillary medicinal substance or an ancillary human blood derivate".

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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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