Suzanne Halliday is the Head of the BSI Medical Devices Notified Body. She has over twelve years of experience as a Technical Specialist and Quality System Auditor for ISO 13485, CE Marking and certain aspects of compliance for Canada, USA, Japan, Taiwan and Australia. Prior to working for BSI she completed a Bachelors and Masters in Science (University of Waterloo) and a Doctorate in Engineering (University of Oxford). She has designed joint replacement implants, spinal and fracture fixation systems. She has also conducted post market clinical investigations on these same types of orthopaedic implants.

Suzanne has developed and delivered numerous presentations at international conferences on Compliance to the Medical Devices Directive, Risk Management, Clinical Evaluations and Investigations, Meeting Essential Requirements with Harmonised Standards, Post Market Surveillance and Vigilance.

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