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U.S. Food and Drug Administration
U.S. Food and Drug Administration
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_i-o-h-software-as-a-medical-device-samd.webp "In partnership with Binah, Voyage81 and IBM Watson Health, Universal Mind is a SaMD “Software as a Medical Device”, extracting heart rate, blood pressure, respiratory rate and hyperspectral imaging. All via a regular smart phone camera.nnBinah, based in Tel Aviv, have completed medical trials in four locations, for FDA medical device approval in 2021 for doctors, hospitals and the global medical community.nnVoyage81, also in Tel Aviv, is a startup founded by the heads of R&D from Mossad,")
_fda-definition-of-a-medical-device.webp "Medical Device Training")
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_the-invasion-of-mobile-medical-apps-a-5-year-outlook.webp "Digital health is a fast-growing space and will shape medical technology innovation of the future. This is an overview about the trends in mobile medical apps today and in the next 5 years. The topics discussed in this lecture include:nn1. The rise of digital health and impact on healthcaren2. Early FDA-approved mobile medical devicen3. Trends in 2014 and 2015n4. Best mobile medical apps in 2014 and 2015n5. Market growth and where the technology is headingn6. Evaluation of medical mobile app cat")
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_frances-richmond-risk-assessment-and-management-tools-part-1.webp "Frances Richmond, PhDnProfessor and Director, Regulatory Science ProgramnClinical Pharmacy and Pharmaceutical Economics and PolicynnIn this second session, Dr. Frances Richmond introduces us to the concepts of Risk Assessment and Management Tools as formal processes within the Regulatory framework we should all be aware of as clinical translational researchers who work with FDA approved drug or devices. Interestingly, she comments that these important regulatory strategies are “not particularl")
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