MAUDE (Manufacturer and User Facility Device Experience)
MAUDE stands for Manufacturer and User Facility Device Experience and is the FDA’s database of voluntary reports of adverse events caused by medical devices. EMRs can fall under the category of medical devices and there are some reports about deficits in EMR CPOE (Computer Physician/Provider Order Entry) related to their ability to choose specific drug dosages for prescribing. You can find MAUDE here.
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