At ICON, we are transforming trials to help bring more cost effective medical devices and diagnostics to market
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Monday, September 24, 2018, 12:00PM - 2:00 PM
Vice President and Global Head Medical Device and Diagnostics Research
The European Union adopted new regulations for medical devices and in vitro diagnostics last year and is currently in the process of implementation. The new regulations fundamentally change not only the process for regulatory approval process for medical technology in the EU, but also will have a dramatic impact on the number of products that will need to undergo review. There will be an enormous impact on all phases of the CE mark process, including pre-market approval, data requirements and post-market surveillance and inspections. The expert panel, with representatives from government, consultants and industry will provide the information you need to more effectively navigate this complex landscape.
ICON is honored to be selected as a finalist for the 2018 Medtech Insight In Vivo Award for Best Medtech Partnership/Alliance in recognition of how our work with Boston Scientific's Rhythm Management (RM) team has set a new benchmark in partnering activity.Register to Attend