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Regulation Combination Products Europe

Arkan Zwick Q&A, Part 2: EU Combo-Product Review Challenges

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Executive Summary

In the second half of a Q&A with Medtech Insight, Croma Pharma executive Arkan Zwick talks about the challenges of getting the drug element of a device-type combination product reviewed in the EU and what combo-product firms have to look out for under the oncoming Medical Devices Regulation. Read the first part of the conversation here.

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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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