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23 24 * PHARMACEUTICAL REGULATORY AFFAIRS IN AFRICA
25 26 27 * PROJECT MANAGEMENT FOR PHARMACEUTICAL PROFESSIONALS
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MEDICAL DEVICES
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AN INTRODUCTION TO
THE MEDICAL DEVICE
DIRECTIVES

Attendance at this event could qualify you for
Fast-track approval for the NSF/DBA Diploma.

Conference Date: 06-07 Dec 2012
Conference Ref: N12-8212
Fee: £1250 + VAT
Venue: The Rembrandt Hotel, London

If you are interested in the NSF/DBA Diploma please email andrea.james@management-forum.co.uk.

Benefits of 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 Legislation

With John Webster, Consultant to the Medical Device Industry

WHO SHOULD ATTEND

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.

If you have any queries please click here to email Andrea James