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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.

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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.