An Introduction to the Medical Device Directives


This seminar provides a detailed introduction to the European Medical Device Legislation. It will explain the Directives and which products are covered, the involvement of Notified Bodies, how to choose one and outline what a manufacturer must do. It will also cover the documentation necessary to apply for the CE Mark

Exhibitors

John Webster Consultant to the Healthcare Industry, Janette Benaddi NAMSA, Theresa Jeary LRQA Notified Body

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