The EU MDR poses tremendous economic and practical challenges for manufacturers. With deadlines looming, lingering ambiguities, and limited availability of notified body support, companies struggle with implementation.
The MedTech Intelligence web seminars assemble key industry experts, notified bodies, and EU MDR consultants to share practical strategies and procedures for EU MDR implementation.
The new EU Medical Devices Regulation (EU MDR) will profoundly affect the medical device market in Europe. Implementation deadlines are rapidly approaching. Companies that have not already made significant progress in planning and preparation may be at risk of losing EU product registrations. With notified bodies and consultants understaffed and overcommitted, help will be hard to find. Anyone can read the regulation, but interpretation remains vague in some areas, and even the best prepared companies have large teams struggling with impact analysis, strategy, budgeting, and implementation.
This two half-day virtual event features presentations and panel discussions by speakers from notified bodies and top medical device companies. Pooling knowledge and strategies will help the industry as a whole better plan for the massive and costly upcoming changes.
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