An Introduction to the Medical Device Directives 2014

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.

SPEAKERS:

Janette Benaddi, Director of Clinical & Consulting, NAMSA

Theresa Jeary, Technical Manager, Medical Devices, LRQA Notified Body