Common Questions and Challenges with Class II UDI Compliance

Medical device manufactures of Class II devices only have a few more months to comply with the UDI Final Rule.  This webinar is a chance to learn from the successes and failures of your peers in the medical device community. You will also get answers to the most common questions manufacturers have about compliance and learn about the challenges other manufacturers are facing.

The discussion will include:

  • Common Questions from Medical Device Manufacturers
  • Challenges Facing Class II Manufacturers
  • Live Q & A Session

About the Presenter:

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.

 

 

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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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