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Home » FDA advisory panel sees heightened risk in connection with GenAI
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FDA advisory panel sees heightened risk in connection with GenAI

Nov. 25, 2024
By Mark McCarty
The first day of the U.S. FDA’s two-day advisory hearing on generative artificial intelligence reflected some of the anxieties attached to this emerging technology, with the phenomenon of hallucinations driving several calls for more stringent regulation of this class of products that might be applied toward other entries in the class of artificial intelligence.
BioWorld MedTech Regulatory Artificial intelligence Digital health U.S. FDA

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