This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Regulatory Affairs, Medical Devices

Update on the EU MDR delay and impact on industry - Panel discussion

Posted by on 30 April 2020
Share this article

With confirmation of the EU MDR delay due to COVID-19, MedTech Summit brought together four industry insiders to discuss the update and the impacts it will have on industry. The video discussion features:

  • Gert Bos, Executive Director & Partner at Qserve Group, The Netherlands
  • Annabelle Bruydonckx, Counsel at Simmons & Simmons LLP, Belgium
  • James Whitehead, Patient Safety Medical Device Lead at AstraZeneca, UK
  • Vladimir Murovec, Supervising Associate (Healthcare & Life Sciences) at Simmons & Simmons, Belgium

Rebecca Brady, Senior Conference Producer at Informa Life Sciences, led the discussion, which you can watch in full below (or here):

Share this article

Sign up for our MedTech Monthly newsletter

Get the latest content and updates straight to your inbox