Learn More About CE Marking And The Medical Device Directive

Enews - 25 March 2014

Medical device regulatory training from world-leading experts

You are invited to watch our free taster webinar about CE Marking and the Medical Device Directives.

Our Medical Devices CE Marking training courses will help you learn more about current European requirements. This taster that will show you a few slides from the course and is hosted by Suzanne Halliday, our Head of Training for Healthcare.

BSI-Suzanne-HallidaySuzanne has over ten years of experience as a Technical Specialist and Quality System Auditor for ISO 13485 and CE Marking. 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.

Seen the webinar and want to learn more?

Browse our training courses to find the right one for you, or call us to discuss your training options: +44 845 287 4388.

Still have questions on IEC / EN 61010-1 3rd Edition Compliance (Safety requirements for electrical equipment for measurement, control and laboratory use)?

Download our Q&A sheet to find out how BSI can help you comply.