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Equity and AI Governance at Academic Medical Centers

Equity and AI Governance at Academic Medical Centers
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A Critical Analysis Of FDA Human Factors IFU Guidance For Drug Delivery Devices

A Critical Analysis Of FDA Human Factors IFU Guidance For Drug Delivery Devices
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Your Digital Health Regulation Questions Answered - Healthcare

The U.S. Food and Drug Administration's (FDA) Center for Devices and Radiological Health (CDRH) regulates medical devices, including software-as-a-medical-device (SaMD).

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New FDA Guidance on AI and Medical Products | Troutman Pepper

New FDA Guidance on AI and Medical Products | Troutman Pepper
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FDA Charts Course for Regulating AI Used in Medical Products | McDermott Will & Emery

On March 15, 2024, four of the US Food and Drug Administration’s (FDA) medical products centers released a joint paper, titled “Artificial Intelligence & Medical Products: How CBER,.

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