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Scrip Regulatory Affairs
In praise of the CE marking, but medtech's worst fear is still alive
06 July 2010
Ashley Yeo

The European Medicines Agency review meeting in London on 30 June passed with scarcely a mention of devices and diagnostics.

This was perhaps as expected, given that the meeting, held to examine the outcomes of the assessment of Ernst & Young's Evaluation of the EMA report (January 2010), was focused mainly on the centralised procedure, resources available and future sustainability...

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