Mireille De Cré and John Brennan
The European legislation which governs medical devices is undergoing continual evolution and this article analyzes and highlights the importance of all stakeholders’ participation in standards development.
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Please note that this article first appeared in the June 2011 issue (volume 3, number 3) of the Global Forum and that copyright to this article is held by the DIA.
28 September – 2 October 2012 | Vienna, Austria
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