This webinar is perfect for you if you're a medical device manufacturer or health care distributor.
The FDA's new Unique Device Identification (UDI) regulation says that if you manufacture medical devices, you're required to comply on or before September 24th, 2020.
But are you ready to embrace a UDI system?
Watch our on-demand webinar and learn how to develop a UDI roadmap and implementation strategy.
You'll also learn how:
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