Apply AI: Piloting AI-based image screening in medical centres

Expected Impact: na Expected Outcome: Outcomes and deliverables One or more proofs-of-concept of replicable, scalable cloud-based AI/GenAI systems for analysis of medical imaging data in a healthcare setting, with demonstration of the role of the clinicians in validating AI/GenAI findings and reports showcasing seamless integration of the system into clinical workflows. Evidence-based analysis of (cost-)efficiency of the piloted solutions for healthcare systems for regulatory and HTA purposes. Two or more events or workshops organised per year and per project for the European network of AI-powered advanced screening centres. The agenda should include lessons learned from the project activities, as well as other items relevant to the network. Participant satisfaction rates should be measured for the events and workshops. Medical centres in the consortium joined the European network of AI-powered advanced screening centres under the Apply AI Strategy. A plan for obtaining regulatory approval for application of the AI/GenAI solutions in real life scenarios and clinical settings. This includes the required risk management and compliance activities, as well as clinical evaluation plans and post-market clinical follow-up. Detailed data protection and cybersecurity plan, with measures to secure sensitive health data, mitigate cybersecurity risks, and comply with EU legal and ethical frameworks. Sustainability plan for the uptake of the systems across the EU. Stakeholder engagement a…bron

• Implementatie van schaalbare cloud-gebaseerde AI/GenAI-systemen voor analyse van medische beeldvormingsgegevens in gezondheidszorg
• Systemen moeten Europese betrouwbare en veilige AI/GenAI-algoritmen gebruiken
• Veilige, privacybeschermende cloudomgeving vereist voor gezondheidsgegevensanalyse
• Naadloze integratie in reguliere klinische workflows van betrokken zorginstellingen
• Interoperabiliteit met gezondheids-IT-infrastructuur (EHR, PACS, RIS) moet worden aangepakt
• Technische en klinische validatie van systemen in echte gezondheidszorginstellingen
• Focus op ziektegebieden kanker en cardiovasculair
• Bewijs van kostenefficiëntie voor regelgeving en HTA-doeleinden

De eisen uit de regeling. Uw situatie bepaalt of u voldoet; dit is geen beschikking.

Zoals beschreven door de verstrekker. Onvolledig? Controleer altijd het officiële loket.

Aanvraag via Funding & Tenders Portal; evaluatie volgens call document sectie 8-9; voorwaarden in call document secties 5-10.

Geen openbare bronnen beschikbaar.