Join Jay Crowley, FDA’s Unique Device Identification Architect to Learn About UDI Final Rule

 

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

 

 

 

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  • Clintrak - Jeffrey D. Coffin
    I have had the great pleasure to work with Bob for 5 years in his position of VP of Quality at Fisher Packaging Services while I acted as Director of Quality services at a sister…
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