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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.

Details

Course overview

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.

Why you should attend

This seminar will provide key guidance and interpretation of the changes to the regulation and will be of value to all those who are involved with placing a medical device on the market, and anyone who requires an essential overview of the new medical device regulation and its impact on the industry and working practices.

Prices

GBP EUR USD Standard 1499 2099 2338 Early 1299 1819 2026 Excluding VAT @ 20.00% Book by 7 Aug to get the early booking price shown above.

Contact

Leigh White
info@management-forum.co.uk

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