Navigating FDA’s Draft Guidance for AI-Enabled Medical Devices

Navigating FDA’s Draft Guidance for AI-Enabled Medical Devices

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Medical Devices and Diagnostics Industry
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A look at how FDA's new draft guidance outlines recommendations for lifecycle management and marketing submissions of AI-enabled medical devices, emphasizing a total product lifecycle (TPLC) approach to address transparency, bias, data management, and risk management throughout the device’s development, deployment, and ongoing monitoring.