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UDI

medical device testingIn 2007, the FDA was tasked with developing a system for identifying and analyzing the risks associated with medical devices after they entered the market. The Sentinel Initiative was launched in 2008 in an effort to track the necessary information in a federal database. In February, the most advanced form of the Sentinel Initiative became fully operational, yet there are some concerns that the tracking and monitoring capabilities of the current system do not go far enough.

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