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24/09/2013
The European Commission adopted two measures to further strengthen the safety of medical devices under the current legislation. Those measures are Commission Implementation Regulation on the designation and the supervision of notified bodies under Council Directive 90/385/EEC on active implantable medical devices and Council Directive 93/42/EEC on medical devices, and a Recommendation on the audits and assessments performed by notified bodies in the field of medical devices.
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