Getting Ahead Of The Game: Implementing Unique Device Identification Without Derailing Production
For the sake of patient safety, the ability to track and trace medical devices at a global level is paramount.
Currently there is no single global regulation for uniquely identifying medical devices in the supply chain. This means recalling devices is less efficient and more complex than it could and should be, negatively impacting patient safety and confidence.
PRISYM ID’s “Getting Ahead of the Game” whitepaper covers all the essential aspects of UDI; including key benefits for both patients and medical device manufacturers. The whitepaper also discusses how manufacturers can effectively plan their future labeling operations strategy by implementing a validated, secure label lifecycle management solution that complies with the FDA’s UDI directive, without derailing production.