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Published on | 51 minutes ago
Programmes HealthThe European Rare Diseases Research Alliance (ERDERA) will launch its 2026 joint transnational call 'Resolving unsolved cases in rare genetic and non-genetic diseases' on 10 December 2025. The goal of this call is to solve Undiagnosed Rare Genetic diseases and to address complex, multifactorial Rare Non-Genetic diseases by identifying causative variants in patients with no molecular diagnosis after prior genetic or genomic testing and providing diagnostic clarity for conditions of unknown or mixed pathogenesis.
Research Foundation Flanders (FWO) plans to participate in this call. More information on available funding for researchers based in Flanders and on how to apply will be published on FWO's website once the call is launched. Deadline for the submission of pre-proposals is 12 February 2026. Questions on available funding by FWO? Contact europe@fwo.be.
More information on the call, its conditions and how to apply will be made available soon on the ERDERA dedicated webpage. Interested in applying? Join the information webinar on 16 December 2025 here.
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The Department of Economy, Science and Innovation of the Flemish government coordinates the Horizon 2020 Coordination and Support Action SAPHIRe, which started on 1 December 2018. The aim of the project is to secure the adoption of personalised medicine in all European regions, including sparsely populated and remote regions and regions with different innovation capacities.
The activities of SAPHIRe are complementary to the smart specialisation partnership on personalised medicine – S3P4PM, which is also coordinated by the Department of Economy, Science and Innovation.
