The New Medical Device Regulation will help you prepare for these changes and operate successfully in Europe. The program will provide in-depth coverage of 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, the role of authorized representatives, economic operators, and the implications of Brexit. There will be plenty of opportunities to discuss the implications of the changes with our expert faculty, and you will gain valuable guidance on the successful implementation of the regulatory changes for your company products.

Website: https://10times.com/new-medical-device-regulation-ivd-regulation

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