The goal of UDI is to help improve patient safety by enabling better traceability of medical devices consumed. For the ‘labeler’, UDI will help improve internal processes, bolster master data quality, and provide more accurate reporting and visibility related to product recalls and counterfeit devices. But it can be a significant challenge to meet these regulations.
Today’s Success Spotlight
The adoption of UDI policies around the world presents a major challenge for medical device manufacturers trying to understand and comply with this flurry of country-specific regulations. As compliance deadlines approached, a leading global IVD device supplier realized they had an opportunity to drive product master data management and best practices as part of their UDI compliance initiatives.
Want to learn more about how this global medical device supplier met their regulation requirements with innovation, read the full case study here!