Peter Rose and Terry Gustafson will be attending this specialist MDR workshop. The aim of the day is to lead delegates through the development of a time-critical action plan for keeping medical devices on the EU market using proven strategies and tactics. At this workshop, delegates will develop:

  • Advanced strategies to effectively work with notified bodies.
  • Insightful game plans for compiling the data required to certify products.
  • Recommendation plans to heighten awareness of the urgency to take action and gain support from senior leaders (CEO, COO, CQO, CFO, Chief Legal Officer, etc.).

Walk away with practical solutions to successfully prepare your company for the fast-approaching regulation deadline of May 26, 2020