September 5, 2024
White Paper
Navigating a smooth course through the Unique Device Identification journey
How data integrity mitigates risk, ensures quality, and positively impacts UDI across the medical device product lifecycle
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Unique Device Identification (UDI) systems are being implemented globally. Whether it’s the USA’s FDA UDI, Europe’s EU MDR, India’s CDSCO, or China’s NMPA, countries from north to south and east to west are adopting UDI systems. UDI improves patient safety, enhances the traceability of medical devices, and streamlines regulatory processes.
To manage these evolving regulations globally, medical device organizations need to focus on a cloud-based approach to labeling and packaging and automate data management to ensure accurate labeling and UDI integrity.
In this whitepaper we look at how to navigate this complex journey from the start, how to circumnavigate UDI around the world with each region’s nuances, and how future proof cloud solution choices can set the right direction for medical device organizations to meet these labeling challenges.
Download this whitepaper to see how labeling can support your UDI journey globally.
- Cloud
- Regulatory
- UDI
- Supply Chain
- Labeling