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Working together to deliver innovative medical care

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Karen A. Newman

The FDA says it has a way to cut nearly in half the time it takes the agency to review most premarket approval applications for high-risk or novel medical devices. In a world in which new consumer products and new versions of popular products from cell phones to sports drinks hit the market at a breathtaking pace, there is always someone, somewhere, waiting for the next breakthrough in medicine or medical devices that could save or greatly improve his or her life. Cutting as much as 150 days off the preliminary approval process for innovative medical devices seems like a step in the...Read full article

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