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 […]
We have recently discussed the standards and regulations regarding the upcoming UDI ruling and how proper implementation is key. The FDA, who oversees that these standards are met, appropriately shared some insight on the ruling and a test-case example on why it is such an important decision for the health care system. Please read the […]
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A great article from Med Device Online regarding the recent and upcoming changes to UDI compliance. These new regulations coming into affect will ensure proper information and identification is attainable to the consumer for proper use and understanding of the product. To view the full article click the link below: http://bit.ly/1DwOK0S