With the second phase of UDI compliance dates coming in less than a year ( September 2015) for medical devices to require UDI labeling; it is imperative that organizations  continue to advance their preparations to begin implementation of these labeling requirements and that preparation begins with populating the UDI database known as GUDID(Global Unique Device Identification Database).

It is the responsibility of the device manufacturer to generate and update the required information into the GUDID while the FDA’s Center for Devices and Radiological Health maintains that database.

There are numerous steps in order to begin this process and Med Device Online created a great foundation to begin the implementation.  Please click the link below to read more.

http://bit.ly/1BkgP9x