Introduction

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.

.Understand the Medical Device Directives
.Learn the Role of a Notified Body
.Know what a Competent Authority Expects
.Hear More on Classification
.Understand Conformity Assessment Procedure

Useful links

• Further event details More information about the event

Venue

Rembrandt Hotel

Rembrandt Hotel, 11 Thurlow Place, London, SW7 2RS, United Kingdom

Contact information

Barbara Mcmanus
Management Forum Ltd
014 8373 0071
Contact us by email

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