Changes in medical device regulation in Europe - What you need to know

Chairpersons: R. Byrne, S. Oktay

Learning Objectives

  • To learn what is new and different with the 2017 medical device regulation
  • To learn how the European Medical Device Regulation compares with regulations in other geographies
  • To learn about physicians involvement in the approval processes for coronary stents

Presentations available when logged in:

  • Session objectives
  • The new 2017 European Medical Device Regulation (MDR) - Key developments and impacts
  • Changes in device regulation in the United States
  • Industry perspective on regulation and access to innovation in Europe
  • Physician involvement in the regulation of coronary stents in Europe - Experience so far
  • Sesssion evaluation and key learnings