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Further guidance is needed to protect patients from "sycophantic" genAI documentation outputs that influence medical decisions, and researchers are asking the FDA "to clarify its oversight before summarization becomes a part of routine patient care."
BRANCHBURG, N.J., Dec. 4, 2023 /PRNewswire/ -- The First ever CE mark was awarded to a Medical Device sterilized using Chlorine Dioxide gas following new MDR ...
Lunit's INSIGHT MMG, an AI tool for breast cancer screening, matches human radiologists' accuracy, revolutionizing diagnostics and prompting integration into standard protocols.
Neurovalens successfully secured 510(k) clearance from the FDA on October 27, 2023 for its Modius Sleep device with relation to treatment of insomnia and/or anxiety. The clearance was...
AI Roundup: Tech experts from India have been named to a new global advisory body announced by UN Secretary General. Quibim partners with Philips to launch new AI-based imaging and reporting tools.