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UDI Crunch Time: Preparing Your Data for Submission

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Webinar_UDI_crunchtime

Medical device labelers face a number of challenges as they work to comply with the UDI Rule, including electronic submission of UDI data records to the FDA’s Global Unique Device Identification Database (GUDID).

Join Reed Tech UDI expert John Lorenc on March 22 to learn how best to prepare your UDI data for submission to the GUDID.

If you would like to attend but have a conflict, please register and you will be able to access a recorded version of the webinar following the live event.

This event is the first of a three part UDI webinar series hosted by Fierce Medical Devices and sponsored by Reed Tech.

March 22: UDI Crunch Time: Preparing Your Data for Submission

April 21: UDI So Far: Lessons for Class II Labelers

May 17: UDI After Submission: Managing the Lifecycle of a UDI Record

We hope you will join us for all three events! In the meantime, please contact us with any questions about this event or UDI and we will be happy to help.

Comments

  • B Casler

    GUDID:
    Labeler organization DUNS and Labeler DUNS.
    DO these have to be 2 different DUNS numbers? DUNS for labeler organization and DUNS for Labelers.
    Can the Labeler organization DUNS be used by the Labelers (note the plural)?