Tag Archives: Medical Devices
FDA Proposes Unique Device Identifier For Medical Devices
July 9, 2012In an effort to improve adverse events reporting, the U.S. Food and Drug Administration (FDA) has proposed that most medical devices distributed in the United States carry a unique device identifier (UDI). A UDI system has the potential to improve … Continue reading
Posted in Health IT | Tagged EHR, EHR Consulting, EHR Implementation, Electronic Health Records, Electronic Medical Records, EMR, Environmental Intelligence, FDA, Health IT, Health IT Policy, Health IT Services, Health IT Standards, Meaningful Use, Medical Devices, Patient Experience | Leave a comment
