FDA nods ADHD test

July 22, 2013

THE US Food and Drug Administration has approved marketing of the first medical device based on brain function to help assess attention-deficit/ hyperactivity disorder (ADHD) in children and adolescents 6 to 17 years old. The device, the Neuropsychiatric EEG-Based Assessment Aid (NEBA) System, is based on electroencephalogram (EEG) technology, which records the frequency and type of electrical impulses given off by neurons.

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Pharmacy Daily | FDA nods ADHD test

FDA nods ADHD test

Other recent headlines

PD breaking news – Top Western Australian talent honoured

Legal action for Montu

Call to unblock wait times

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES