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.(JavaScript must be enabled to view this email address) for an overview of the medical device standards information relevant to your complete portfolio.
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.
Please click here to view this article.
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.