
Regulation
AMA weighs in on FDA’s regulatory proposal for GenAI-based medtech
The American Medical Association submitted comments on the FDA's proposed regulatory framework for generative AI-based medical devices, urging the agency to prioritize safety over speed in approval processes and calling for physician input on clinical performance standards and evaluation criteria for AI-driven medtech.
The source
This brief is a MedIndexer summary of reporting by Medical Device Network. To read the full story, head to the source.
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