Friday, 05th Dec, 2014 | 11:00 AM EST | 04:00 PM GMT

60 Mins

As per FDAs UDI final ruling, GUDID will accept only DI information and it is the responsibility of the medical device manufacturer to maintain the PI information for any future regulatory and quality audits.

Join us to know how Product Identifier information can be effectively maintained with Freyr Identity: a seamless, easy to use, end-to-end solution for UDI compliance and device lifecycle management.

This webinar features;

  • UDI overview
  • DI & PI in detail
  • DI & PI on a package
  • DI workflow in GUDID
  • DI data collection
  • GUDID attributes
  • DI submission process
  • Device lifecycle management

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