Thursday, February 1, 2024

< + > FDA medical device loophole could cause patient harm, study warns

Further guidance is needed to protect patients from "sycophantic" genAI documentation outputs that influence medical decisions, and researchers are asking FDA "to clarify its oversight before summarization becomes a part of routine patient care."

No comments:

Post a Comment

< + > What's behind EHR-induced clinician burnout? And how to solve it?

When evaluating electronic health record systems to minimize documentation burden, usability is always the big challenge, says one informati...