The Food and Drug Administration appears to be taking a proactive and long-term approach toward improving medical-device safety. On April 17, the FDA released its Medical Device Safety Action Plan, in which regulators set out their goals for improving device safety, including tracking a product’s safety throughout its life-cycle and catalyzing innovation that will make devices safer.”Overall, this is a positive step to try to take proactive action to create a better environment for medical devices,” said David Chou, chief information and digital officer for Children’s Mercy Kansas City.

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