AN INTRODUCTION TO
THE MEDICAL DEVICE
DIRECTIVES

Conference Date: 22-23 Oct 2009
Conference Ref: N10-8009
Fee: £1140 + VAT
Venue: The Rembrandt Hotel, London

BENEFITS IN ATTENDING:

• Understand the Medical Device Directives
• Learn the Role of a Notified Body
• Know what a Competent Authority Expects
• Hear More on Classification
• Better Understand Conformity Assessment Procedures
• Comply with Manufacturing Responsibilities
• Gain an Insight into Labelling of Devices
• Discover Medical Device Vigilance
• Consider the Requirements for Quality Systems
• Discuss Drug/Device Combinations
• Plan Your Clinical Evaluations
• Take Away Information on Devices Incorporating Material of Animal Origin
• Gain an Overview of the Revision of the Medical Device Directives

SPEAKERS:

Dr. Brian Matthews - Senior Director, EC Registration, Alcon Laboratories (UK) Ltd.
John Webster - Managing Director, Medical Device Consultants International Ltd. UK

INTRODUCTION

This seminar provides a comprehensive 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, plus the documentation necessary to apply for the CE Mark.

This is an excellent introduction from leading experts in the field.

WHO YOU WILL MEET

Past delegates include personnel from the following departments:

• Regulatory Affairs,
• Pharmacovigilance, Quality
• Assurance and Technical Support.

This seminar will be of interest to all personnel who are new to the medical device industry, all those who intend to place a medical device on the market and anyone who requires an overview of the medical device sector.

Click here to book your place on this important event.