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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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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.

People already use ChatGPT to determine if a doctor's visit is necessary, so AI is already in the decision chain.

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