Programme

2015, February

Have you ever wondered how the European Directives were made? What does “CE” stand for? Or Why do we call Notified Bodies by this name and what their role is?

Medical device manufacturers that sell their products in Europe need to know the answers to these questions. Notified bodies have many responsibilities that extend beyond simply performing product assessments for CE Marking. Join LNE/G-MED North America in its Free webinar, CE Marking and the Roles of Notified Bodies and learn how the Directives, notified bodies, and CE Marking fit together.

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