How to Use All That UDI Data You Submitted
John Lorenc from Reed Tech explains UDI doesn’t end with your submission to the FDA’s GUDID database:
After submission, you’re required to keep your GUDID entries up to date and continue submitting new records as you add to your device portfolio.
Since manufacturers are doing the work anyway, they may as well use the UDI data downstream. Leading device labelers are using the data records they submit to the FDA to update their own internal processes and systems.
UDI data can even form the basis for a Master Data Management (MDM) system.”
In this free event, UDI expert John Lorenc will present how to make your submission to FDA, keep your data up to date, and capitalize on it downstream.
And if you haven’t yet submitted to FDA, you’ll really need to attend.
BONUS! When you register below, you’ll get immediate access to six very popular UDI presentations Reed Tech made for the Medical Devices Group.
>> Forward this link to colleagues who would value this content.