6 Months Until UDI Go Live - Issues in the Life Sciences Industry

 

Learn about the critical issues medical device companies face and what to do about them. This webinar will also give you an opportunity to hear what medical device companies need to be concerned about as they become UDI compliant. You will also get a chance to hear about the compliance methods that have already led to successful UDI compliance.

The discussion will include:

  • Critical issues and resolutions to meet deadline
  • How to make device by device decisions
  • Recent FDA comments
  • Emerging industry best practices
  • Live Q & A session

The featured speaker, Jay Crowley is the Vice President of the UDI Practice at USDM Life Sciences.  Jay was Senior Advisor for Patient Safety in the Food and Drug Administration’s Center for Devices and Radiological Health. Jay developed the framework and authored key requirements for FDA’s Unique Device Identification system.

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Testimonials

  • 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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