Learning Marketplace

7 Rookie Mistakes Made by Medical Device Start-Ups

Considering a Notified Body? Want to learn from other manufacturer's mistakes? BSI's FREE webinar outlines commonly made mistakes by early stage, start-up medical device manufacturers. BSI has helped thousands of companies navigate the regulatory path to achieve CE Marking and entrance into the European Market without costly mistakes, missteps, and myths along the way. Register today and learn from BSI's medical device expertise!

Learning Objectives:

  • Understand the value of being properly prepared when engaging with an EU Notified Body
  • Realize how correctly classifying a medical device impacts its route to conformity
  • Verify the status of subcontractors working in your supply chain
  • Be aware of the requirement for appropriate Post Market Surveillance
  • Additional items

Who Should Attend:

  • Executives from early stage medical device companies
  • Quality Assurance professionals
  • Regulatory Affairs professionals
  • Venture Capital investors
  • Business Development professionals