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Out of curiosity, has any company been able to get any kind of regulatory approval (US, EU, doesn't matter) for an AI-based medical device trained in a federated setup? Has anyone tried this? Is it at all possible given current regulations? Are there any useful discussions / whitepapers / guidelines or whatever on this subject?
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Out of curiosity, has any company been able to get any kind of regulatory approval (US, EU, doesn't matter) for an AI-based medical device trained in a federated setup? Has anyone tried this? Is it at all possible given current regulations? Are there any useful discussions / whitepapers / guidelines or whatever on this subject?
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