The MedTech Conference 2018

ICON is transforming trials to help bring more cost effective medical devices & diagnostics to market

Meet ICON Experts at The MedTech Conference 2018, Booth 300

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Implementation of the New European Medical Technology Regulations: Is Anyone Ready?

Monday, September 24, 2018, 12:00PM - 2:00 PM

Vicki Anastasi

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.

Additional Speakers

  • Moderator: Erik Vollebregt, Partner. Axon Lawyers
  • Michel Marboeuf, Stryker
  • Ibim Tariah, Technical Director, BSI Healthcare
  • John Wilkinson, Director of Devices, Medicines and Healthcare products, Regulatory Agency (MHRA)

2018 Medtech Insight Award

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.

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Scan your badge at Booth 300 to enter the drawing for an Apple Watch 3