FDA Requires Device Manufacturers to Include Information on Pediatric Populations
Wed, 31 Mar 2010 11:21:00 -0500
The U.S. Food and Drug Administration announced today that will begin implementing a requirement that device manufacturers provide readily available information in certain premarket applications on pediatric patients who suffer from the disease or condition that the device is intended to treat, diagnose, or cure, even if the device is intended for adult use.
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