Learning Marketplace

Intro to CE Marking for Medical Devices

Are you thinking about selling your Medical Devices in Europe? Or have your already started on the pathway? Either way you will need a CE Marking to gain access to the 27 countries, with almost 500 million people that comprise the European Union (EU) market. Come join BSI for this informative 1-hour webinar to gain a basic understanding of the CE Marking regulatory process and the impact the Medical Device Directive (MDD) requirements have on marketing a new medical device in the EU. Learn the different medical device risk classifications and when you need a Notified Body. Plus the initial steps to getting started.

Learning Objectives

  • Gain an overview of the EU Marketplace
  • Understand the basic requirements for CE Marking medical devices
  • Know fundamentals of risk classification and routes to conformity
  • Understand the role of a Manufacturer, a Notified Body and other key players

Who Should Attend

  • New or Emerging Medical Device Companies
  • New Regulatory Affairs and Quality Professionals
  • Suppliers; Organizations New to International Medical Devices Markets
  • Marketing Professionals
  • Medical Device VC Investors
  • Persons involved with placing Devices on the Global Markets
  • Medical Device Design Engineers