Integrated virtual-human-twin solutions supporting prevention and diagnosis through validated, interoperable clinical decision tools. This briefing highlights the opportunity at a practical level; the official topic conditions remain binding.
Virtual Human Twins for clinical decision support
Integrated virtual-human-twin solutions supporting prevention and diagnosis through validated, interoperable clinical decision tools.
Core intervention logic
- 1Select the clinical challengeIntegrate multiscale models and health data into Virtual Human Twins
- 2Integrate models and dataValidate decision-support solutions in relevant prevention or diagnostic settings
- 3Validate decision supportAdvance interoperability, usability, trust and clinical adoption
- 4Prepare adoptionIntegrate multiscale models and health data into Virtual Human Twins
How the action works
Select the clinical challenge
More personalised and evidence-based prevention and diagnosis.
Who is it for?
Clinical and biomedical research organisations; Modelling, simulation, AI and data-technology teams; Hospitals, patient organisations, SMEs and technology developers. The strongest consortia will connect these capabilities around a clearly defined need rather than assemble partners only to satisfy formal eligibility.
What does the call support?
Integrate multiscale models and health data into Virtual Human Twins.
Validate decision-support solutions in relevant prevention or diagnostic settings.
Advance interoperability, usability, trust and clinical adoption.
What are the key requirements?
- Clinically driven use cases and measurable added value
- High-quality data, validation and appropriate regulatory planning
- Interdisciplinary integration with end-user and patient involvement
- Action type: Research and Innovation Action (RIA).
A competitive proposal must connect the topic’s expected outcomes to a focused intervention logic, credible partners, measurable results and a convincing route to uptake. Scope, eligibility and all special conditions should be checked against the official topic text before consortium commitments are made.
Timeline and next steps
The topic is scheduled to open on 2 June 2027 and the deadline is 22 September 2027. Prospective applicants should use the preparation period to confirm fit, shape the core concept, identify the capabilities required and build the work plan around the expected outcomes.
EXELIXIS can support call interpretation, concept positioning, consortium architecture, proposal development, impact pathways and coordination of partner contributions.
Official sources
This briefing is an original summary prepared from official EU sources. It is provided for orientation and does not replace the binding call text, General Annexes or Funding & Tenders Portal conditions.