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EUMDR / IVDR: Can You Adapt to a Changing Market?

March 20, 2019 @ 1:00 pm - 2:00 pm EDT


Participants of the live webinar will be eligible for 1 free CPE credit.

Register for the Webcast

Program content:With an abundance of significant changes in medical device and in vitro diagnostics regulations which the European Union is expecting to realize in 2020, manufacturers need to identify ways to protect, maintain and grow in a market that will need to accomodate these challenges. This webinar will describe market forces, help identify critical areas you should consider in your EU MDR / IVDR planning and implementation efforts, and help you navigate the challenges.

Learning Objectives:

  1. Identify elements of change in the European market including changes in regulation and the regulatory ecosystem.
  2. Recognize the impact of regulatory change on the growth of your business.
  3. Determine action steps to combat the urgency of the approaching EU MDR deadline.


  • Marty Zuzulo, Director Compliance Risk, Healthcare & Life Sciences Industry, Grant Thornton LLP
  • Judith O’Grady, Corporate Vice President Global Regulatory Affairs, Integra LifeSciences Corp.

Recommended Field of Study: Specialized Knowledge
Program Level: Overview
Prerequisite: None
Delivery Method: Group – Internet

If you have any questions or encounter any difficulties while enrolling, please contact technical support via phone at +1 877 398 9939, via email at GTWebcast@centurylink.com, or visit our webcasting frequently asked questions page.

If you have any questions regarding CPE credit, please contact CPE support via phone at +1 630 396 5831, via email at CPEEvents@us.gt.com, or visit our webcast CPE information page.

Register for the Webcast


March 20, 2019
1:00 pm - 2:00 pm
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Field of Study
Specialized Knowledge