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March Reg Top Hits: Scrutiny Excitement, EN ISO 13485 Special, And IVD Notified Body Capacity

This article was originally published in Clinica

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Executive Summary

News that the European Parliament, European Commission and Council of the European Union seem to have found a way forward towards deciding the future regulatory pathway for high-risk medical devices saw Clinica’s article on “No More Questions” On Scrutiny As EU Talks Set To Give Notified Bodies Yet More Responsibility race to the number one spot of stories most popular with our subscribers.

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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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