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Elsa” is the FDA’s new anthropomorphized AI tool which, the FDA hopes, will speed up clearances, licenses, and approvals ...
The company announced that the US FDA has expanded the approved use of its oral antiviral drug Mavyret, developed in ...
Sonu, an AI-enabled wearable device, is now approved for use in pediatric patients aged 12 years and older for the relief of moderate to severe nasal ...
The FDA plans to "unleash AI" on new drug evaluations in order to "radically increase efficiency in the review process." ...
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Medical Device Network on MSNFDA grants 510(k) clearance to Viz.ai’s Viz Subdural Plus moduleThe solution automatically labels subdural collections and reports measurements such as thickness, midline shift, and volume.
This story is from the next print edition of MIT Technology Review, which explores power—who has it, and who wants it. It’s ...
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A new article in the Journal of the American Medical Association said the FDA will implement AI into multiple processes.
Leaders of the FDA have published a list of new priorities for the agency. They want to deliver rapidly-approved cures and ...
About 30% of all respiratory tract infections are caused by coronaviruses, leading to widespread illnesses and, in some cases, to epidemic and even pandemic outbreaks, as we experienced with the COVID ...
Augnition Labs, a neurotechnology company developing science-driven tools to advance cognitive health, today announced that ...
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