Answers to Your UDI Questions

The Class II UDI deadline is only a few short weeks away.  Are you ready?  Do you still have questions or concerns?  This webinar is a chance to get YOUR specific UDI questions answered live by the top UDI experts in the country.

The discussion will include:

  • Overview of UDI timeline
  • What the FDA UDI Extension Letter Dated Sep 6, 2016 Means
  • Live Q & A session
  • Next steps for medical device manufacturers

Who should attend?

  • UDI Team Leaders/Members
  • Regulatory Leaders/Teams
  • Manufacturing, Operations and Supply Chain Logistics
  • UDI IT Support
  • Distributors with UDI Submission Responsibilities

 About the Presenters:

Jay Crowley 6Jay Crowley is the Vice President of UDI Services and Solutions 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 the FDA’s Unique Device Identification system.




Gary Saner Reed Tech 1Gary Saner, Sr. Manager of Information Solutions in the Reed Tech Life Sciences group, is a subject matter expert on UDI and other structured content submissions to regulatory agencies. He has over a decade of experience in the Life Sciences industry and has worked for over 30 years in the areas of software development, process management and data conversion.



  • 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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