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Medical device manufactures have about six months to comply with the FDA UDI Rule for Class II devices. This webinar is an opportunity to hear about the hurdles some device manufacturers have faced on the road to compliance and how they achieved their goals. You will also get answers to the most common questions our UDI compliance experts receive. Participants will also come away with what they need to do now to ensure UDI compliance.

The discussion will include:

  • Common Issues Med Device Manufacturers Face with Compliance
  • Top Questions Med Device Manufacturers Have
  • What Class II Manufacturers Need to Do Now
  • Live Q & A Session

About the Presenter:
Jay Crowley

Vice President of Unique Device Identification 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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