Did you forget something on your premarket approval application? Check it twice, because the rules have changed…again. The FDA is now requiring manufacturers of medical devices to include pediatric patient information with all premarket approval submissions. The Agency has even said that they may withhold approval of any applications missing such data, until the required [...]
Archive for April, 2010
FDA asks Device Makers…But, what about the kids!?!
Posted by Brad Ryba in Thursday, April 1st 2010
Topics: Pediatrics
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