Proposals must meet all of the following scope criteria:
• Core research focus on enabling or contributing to the destination “Developing and using new tools, technologies and digital solutions for a healthy society”.
• Development or repurposing of ethical, trustworthy, robust Generative AI models directed at advancing predictive and personalised medicine.
• Use of large-scale, high-quality multimodal biomedical data (real and/or synthetic) with justification of data choice for model training and optimisation.
• Implementation of at least two distinct proof-of-concept use cases in different medical fields, demonstrating added scientific and potential clinical value relative to existing methods.
• Active engagement of potential end users in model lifecycle (design, adaptation, testing) and consideration of sustainability aspects.
• Creation or adaptation of rigorous evaluation methodologies addressing performance, robustness, alignment, bias/confounding, explainability, usability and ELSI aspects, building on established European guidelines (Trustworthy AI, Responsible Use of Generative AI, etc.).
• Full compliance with FAIR data principles and GDPR requirements, adopting best practices from European research infrastructures.
• High standards of transparency and openness: open-source code where feasible; detailed documentation of model assumptions, processes and data management.
• Demonstrable EU added value: involvement of EU and Associated Country industrial AI developers (including startups), fostering open strategic autonomy.
• Exploitation of synergies with other Horizon Europe/Digital Europe actions and data platforms (missions, partnerships, EU data spaces, EOSC, EBRAINS, etc.) without focusing on building new infrastructures.
• Inclusion of social sciences and humanities expertise to ensure research relevance, societal impact and responsible innovation.
• Optional but encouraged utilisation of AI factory resources; optional collaboration with JRC for regulatory science and pre-normative frameworks post-approval.
• Allocation of budget for cross-project networking, joint meetings and exchange of best practices; clinical studies detailed in annex if applicable.