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Description
This trans-national call supports international collaborations within personalised medicine. The focus is on testing and demonstrating new data-driven solutions for information-driven treatment and management of chronic diseases, especially where patients have multimorbidity (two or more chronic diseases). Vinnova finances Swedish participation in the joint call executed under EP PerMed.
Funding Amount
- For Swedish parties: Up to SEK 3 million for one Swedish party over up to three years.
- If two or more Swedish parties participate in the same consortium, Vinnova may fund up to SEK 5 million total for the Swedish side.
Submission Deadlines
- International opening: 1 October 2025.
- Swedish national application opens: 8 October 2025.
- Last date for joint consortium submission (Step 1) to EP PerMed: 20 January 2026 at 14:00 CET.
- Step 2 full-proposal deadline to EP PerMed: 27 April 2026.
- Last date for parallel Swedish application (Step 2) to Vinnova: 5 May 2026.
- Decision (Step 2) expected: 1 September 2026.
- Project latest start date: 29 January 2027.
- Project maximum completion date: 29 January 2030.
Submission Conditions
- The project must be a trans-national consortium comprising at least three project partners from at least three participating countries. At least one Swedish applicant must participate.
- The consortium must include at least one company and one clinical partner (such as a health-care provider) as part of the Swedish participation.
- Swedish applicant must submit a parallel national application to Vinnova in addition to the international joint submission.
- The costs must relate to the Swedish legal entity and be recorded in Sweden as per Vinnova’s eligibility rules.
- Eligible cost types include personnel costs, equipment, land/buildings (if not regular business premises), consulting/licensing, other direct costs, overhead (indirect) up to 30% of personnel costs (higher for universities/research organisations).
- State aid rules apply for Swedish economic actors.
- The international consortium must follow EP PerMed eligibility (minimum three partners from three countries; at most two funded partners per country in most cases).
Eligible Types of Businesses
- Swedish actors eligible: enterprises (companies), public sector organisations, academia (universities, colleges, research institutes), non-governmental organisations.
- If more than one Swedish organisation participates, one must coordinate the Swedish participation.
- International consortium must include private sector (industry/SME), clinical/health-care partner, academic/research, etc. Patient/citizen-representing organisations may also participate (under EP PerMed rules) in some cases.
Eligible Countries
- For the Swedish national part: Swedish legal entities are eligible. The international part requires partners from at least three different participating countries (including Sweden).
- Participating countries in the EP PerMed call include many European Member States/Associated Countries.
Expected Outcome
- The funded collaborations should result in innovations (products, processes or services) for personalised medicine that can be tested and demonstrated in near-real-world environments (e.g., healthcare settings), especially addressing chronic diseases and multimorbidity.
- Enhanced use of multimodal health data and advanced analytics (AI/ML) to drive information-driven personalised treatment and care pathways.
- Improved management of patients with chronic conditions through innovations in monitoring, therapy decision-support, remote care, combination therapies, and transitions in care settings.
- Strengthened international collaboration in personalized medicine, linking industry, clinical care, academia and public organisations.
Scope
- Eligible themes include solutions addressing:
- Detection or characterisation of multimorbidity in patients with ≥2 chronic diseases.
- Diagnosis, follow-up or monitoring of disease progression, including relapses/exacerbations.
- Transition from inpatient to outpatient care via remote monitoring or self-reporting using medical devices or other solutions.
- Decision support for treatment strategies (e.g., medication type & dosage).
- Monitoring and management of combination therapies (including drug combinations) to increase effectiveness, reduce side-effects, and reduce harmful drug interactions.
- A clear strategy for collection, processing and use of multimodal health data, applying advanced data processing such as AI/ML where relevant, must be included.
- A holistic system perspective with integration of six “systems dimensions”: knowledge integration; technologies/products/methods/processes; use of infrastructures; business and value models; policies/regulations; organisation/behaviour/values.
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