New Medical Device Regulation 745/2017 (MDR)

Open Letter on the Implementation and Readiness Status of the New Medical Device Regulation 745/2017 (MDR) Critical review of the new Medical Device Regulation from Medtech Europe. Source: https://www.linkedin.com/feed/update/urn:li:activity:6525149926949781504  

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Artificial Intelligence: Who is Responsible if an Algorithm is Mistaken (in German)

Intelligente Maschinen fällen in heiklen Fragen oft präzisere Urteile als das geschulte Fachpersonal. Doch wer ist verantwortlich, falls etwas schiefgeht? Read more: amp.handelsblatt.com/unternehmen/it-medien/kuenstliche-intelligenz-wer-traegt-die-verantwortung-wenn-der-algorithmus-sich-irrt/23828718.html

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Interoperability of Electronic Health Records in Europe: Facilitating Cross Border Cooperation | EEHR

Have you heard of European electronic health records (EEHR) exchange format yet? — Read on www.himssconference.org/updates/interoperability-electronic-health-records-europe-facilitating-cross-border-cooperation

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FDA: Digital Health Policy for Prescription Drug Pricing

New prescription drug-use related software proposed by FDA will help companies and develop an efficient pathway to help increase safety and effectiveness. Read on: www.natlawreview.com/article/significant-fda-digital-health-policy-development-prescription-drug-sponsors

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EU News: Tender for Clinical Practice Guidelines (CPG) and Clinical Decision Support Tools (CDSTs)

European Reference Network: Clinical Practice Guidelines (CPG) and other Clinical Decision Support Tools (CDSTs) — Read on etendering.ted.europa.eu/cft/cft-display.html;eTenderingPublic=0kVGmcqTLa8xpic1H9nFAzo1BcwyFyk7G_CUr0-QG7ag_XNCvGqM!629740168

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NIH Global mHealth Grant

Mobile Health: Technology and Outcomes in Low and Middle Income Countries (R21 Clinical Trial Optional) The purpose of this Funding Opportunity Announcement (FOA) is to encourage exploratory/developmental research applications that…

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