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BioWorld - Sunday, April 19, 2026
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Home » Device makers wary of FDA guidance for AI-enabled software functions
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Device makers wary of FDA guidance for AI-enabled software functions

April 21, 2025
By Mark McCarty
The U.S. FDA’s January 2025 draft guidance for AI-enabled device software functions has not fared well in terms of industry response. Two major trade associations argue that the draft is at least somewhat redundant with existing agency guidance.
Medical technology Regulatory Medical devices Digital health Artificial intelligence U.S. FDA Policy

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