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Regulators begin to shape tougher future for device manufacturers

This article was originally published in Clinica

Executive Summary

The first European Commission experts working group meeting on the forthcoming review of the Medical Devices Directive (MDD) was held in Brussels on April 3 and 4. Discussions there, and in more public meetings, indicate that manufacturers will have to meet tighter safety requirements to assuage critics who believe the Medical Devices Directive is not a strong enough legal instrument for high-risk devices.





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