Recent Cases Dec 18, 2020
The FDA accepts diaMentis Technology to Diagnose Mental Health Issues
Quebec-based medical technology developer diaMentis announced on December 17, 2020, that its mental health diagnostic technology has been accepted in the U.S. Food and Drug Administration (FDA) Breakthrough Devices Program.
Once approved, diaMentis technology could provide primary care physicians and psychiatrists with an objective method for diagnostic decision-making, especially for patients suffering from bipolar disorder or schizophrenia.
There are currently no tools available to assist with mental health diagnoses anywhere in the world. This FDA Breakthrough Devices Program acceptation is an important recognition because, at the moment, diagnoses in this field are based solely on observation of clinical signs and symptoms and can take, in some cases, up to 5 or 7 years to be confirmed.
To read the full press release, click here
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