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Event Details


New Medical Device Legislation

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Who should attend?

Personnel from the following departments: Regulatory affairs Clinical studies Vigilance PMS Quality systems Technical support and business development.



This is a period of great change, uncertainty and opportunity within the medical technology and diagnostics sectors. This seminar will help you prepare for these changes and operate successfully in the changed environment in Europe. The seminar will cover in depth the new regulations and how they will be implemented by Member States and Notified Bodies. You will hear the latest thoughts on clinical development, safety monitoring and the implications of Brexit.

This is a seminar you cannot afford to miss as you put in place your strategies for the new environment.



GBP EUR USD Standard 1399 1958 2182 Excluding VAT @ 20.00%


Leigh White

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