CE Marking – An Introduction to the Medical Devices Directive

Published: 1-Mar-2013

12 - 13 March 2013

Two-day course

Birmingham, UK

The course will include all the major features of the Directive including, among others, product classification, conformity assessment routes and Technical Files including the Essential Requirements. The prime focus of this course will be on the Medical Device Directive, but will of course include reference to the IVD and AIMD directives.

Organiser: High Edge Consulting

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