New Regulations for Medical Devices and IVDs in Europe
During a period of change and opportunity within the medical technology and diagnostics sectors, this seminar will help you prepare and operate successfully in Europe and the UK post Brexit. The programme will provide in-depth coverage of the new regulations and how they will be implemented by member states, the UK and Notified Bodies. You will hear the latest thoughts on clinical development, safety monitoring, the role of authorised 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 successful implementation of the regulatory changes for your company products.
This is a seminar you cannot afford to miss as you put in place your strategies for the new environment.