UDI IMPLEMENTATION – The Key To Unlock Personalized Medicine?

FDA Report “Coordinated Registry Networks to Bridge Clinical Care and Research”

The implementation of Unique Device Identification (UDI) is having a profound effect on Med-Tech manufacturers, healthcare providers, regulators and ultimately the patient. The 7-year compliance timeline reached its second milestone on October 24, 2015. As of that date the labels and packages of implantable, life-supporting and life-sustaining devices must bear a UDI and date. Furthermore, software that is classified a life-supporting or life-sustaining device must include a UDI. In addition, FDA’s new report: “Coordinated Registry Networks to Bridge Clinical Care and Research” calls for the adoption of UDI in patient identification across the entire device life cycle.

Could UDI be a key that unlocks the potential of personalized medicine for the masses?

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