UDI Lessons Learned: Keys to Gaining and Sustaining Compliance
In an effort to improve the quality of information in medical device adverse event reporting, reduce recalls and improve patient safety, the United States Congress passed legislation directing the FDA to develop regulations establishing the unique device identification (UDI) system for medical devices.
How are you supporting this new regulation? And are you prepared for regulations of the future?
During this webinar entitled “UDI Lessons Learned: Keys to Gaining and Sustaining Compliance”, you will learn:
What’s critical after the UDI deadline
UDI impacts far more than labeling and tracking - what you need to know
Preparing for GUDID submission may be harder than you imagine