How Can We Use the FDA UDI Standards for Medical Devices (On Demand Webinar)

FDA UDI is used to mark and clearly identify medical devices and certain combination products within the healthcare supply chain, submit required information to a central repository of information by medical device manufacturers, foreign and domestic, for products sold in the US.

In 2015 FDA UDI compliance will be mandatory for Class II Implants and Life Supporting /Sustaining Devices. 2015 will also see the proposed implementation of UDI by the EU.

Considering these key milestones ArisGlobal presents ‘How can we use the UDI standards for medical devices’ on demand webinar.

Attend this webinar catered towards Medical device manufacturers and gain insight into:
a. The current status of the UDI standards
b. The approach that device manufacturers must take
c. The practical concerns of device manufacturers with respect to the standard
d. The road ahead for UDI


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