Watch

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

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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