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You Snooze, You Lose: Tips To Stay On Top Of Impending Wave Of EU Regulatory Change

This article was originally published in Clinica

Executive Summary

All manufacturers will need to review their product portfolios to determine which products will remain on the market in Europe under the new Medical Device Regulation. The next step will be to prioritize which of these products should be brought under compliance with the MDR first, then ensure timely assessments by notified bodies.

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