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EU experts give go-ahead for high-risk device database

This article was originally published in Clinica

Executive Summary

The European Commission's Medical Devices Expert Group endorsed at its meeting last week on April 7 and 8 the industry-led project to develop a database of information on high-risk medical devices to be made available to medical professionals (see Clinica No 1052, p 3). The meeting agreed that the pilot project should also contain information on high-risk in vitro diagnostics and on active implantable medical devices.

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