Watch Now

The first UDI compliance deadline is less than a year away. (September 24, 2014 for class III devices.) Jay Crowley, former FDA Senior Adviser for Patient Safety will outline what the UDI final rule means for medical device companies, share his tips for successful UDI compliance and address industry concerns. A live Q & A session at conclusion of webinar.

The discussion will include:
  • Outline what the UDI final rule means for medical device companies
  • Tips for successful UDI compliance
  • Address industry concerns
  • Live Q & A session
Who should watch?

Medical Devices Manufacturing Companies - Manager/ Engineers/Director/ VP of:
  • Compliance
  • Quality
  • Software Engineering
  • Research and Development
  • Product Development
  • Regulatory Affairs
  • And C-Level Managers
Want our experts to work on your project?

Take the first step towards creating more value with USDM today.

Connect Now

We use cookies to understand how you use our site and improve your experience. This includes personalizing content and advertising. Learn more.