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News

October  2007

Achieving Medical Device Approval in Europe, 28 and 29 November 2007 :

Organised by Informa Life Sciences on 28 and 29 November in Boston, USA, this conference introduces the differences between American and European regulations, as well as the evolution of the latter. Role and responsibilities of the Competent Authorities and the Notified Bodies, technical documentation, clinical data, post-marketing surveillance are amongst the topics covered.

Marc-Henri Winter, the director of the subsidiary G-MED North America will hold a conference on November,28th on the ongoing review of directives relating to medical devices (93/42/EEC) and active implantable medical devices (90/385/EEC).