Are you done with UDI? Or is it just the beginning?
On Demand Webinar
Leverage UDI to Accelerate Product Quality and Safety
The FDA is intent on significantly improving device evaluation and decision-making through the adoption of Unique Device Identification (UDI) across the device ecosystem. The value of UDI resides in the ability to optimize meaningful data collection and analysis. Once UDI is fully implemented as part of a company’s global business operation, opportunities for improving quality, streamlining regulatory reporting and driving innovations forward are finally possible.
Watch this 60-minute webinar and learn more about:
Implications of UDI on patients, providers and manufacturers
Ability to leverage UDI information in global regulatory strategies
Value of managing the device identifier and production identifier