top | item 39428091 (no title) macilacilove | 2 years ago In the EU if a software is influencing diagnosis decisions of a doctor in any way it needs to be registered as a medical device software. Probably a similar regulation can be expected in the United States too. discuss order hn newest JTyQZSnP3cQGa8B|2 years ago From my own experience, most medical software is sold in the USA and must be certified by the FDA which is equivalent to the CE process. amelius|2 years ago People already use ChatGPT to determine if a doctor's visit is necessary, so AI is already in the decision chain.
JTyQZSnP3cQGa8B|2 years ago From my own experience, most medical software is sold in the USA and must be certified by the FDA which is equivalent to the CE process.
amelius|2 years ago People already use ChatGPT to determine if a doctor's visit is necessary, so AI is already in the decision chain.
JTyQZSnP3cQGa8B|2 years ago
amelius|2 years ago