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Modernizing the FDA Premarket Approval Process for Medical Devices (ReachMD) View |
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BioPractice : FDA’s Premarket Requirements for Medical Devices (BioPractice) View |
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BioPractice FDA’s Premarket Requirements for Medical Devices (BioPractice) View |
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MDUFA IV: Digital Health – A Program Update (U.S. Food and Drug Administration) View |
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What Students Need To Know About Medical Device Regulations. (British BioMedicine Institute) View |
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MDUFA IV and Beyond: Video Reports (U.S. Food and Drug Administration) View |
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Regulating AI Adaptation: An Analysis of AI Medical Device Updates - ArXiv:2407.16900 (Academia Accelerated) View |
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Regulating AI Adaptation: An Analysis of AI Medical Device Updates - ArXiv:2407.16900 (Academia Accelerated) View |
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FDA eSTAR - General Info - #1 in the 510(k) eSTAR series (Medical Device Academy) View |
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510(k) Submission Predicate Selection Webinar - Updated for 2022 (Medical Device Academy) View |