Shaping the future of global rare disease research: Join the 2nd International Conference on Clinical Research Networks

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ERDERA – the European Rare Diseases Research Alliance – is pleased to announce the upcoming2nd International Conference on Clinical Research Networks (CRNs) for Rare Diseases, co-organised in collaboration withRare Disease International and theInternational Rare Diseases Research Consortium (IRDiRC).

The conference will take place on9–10 December 2025, in ahybrid format, welcoming both in-person and virtual participants from across the globe. As in-person places are limited, online participation is strongly encouraged.

Building on the success of the inaugural edition in 2022—organised by ERDERA’s predecessor, EJPRD, alongside IRDiRC—this second edition will once again convene a wide range of international experts, including researchers, clinicians, patient advocates, industry representatives, policymakers, and funders to strengthen the collaborative ecosystem that underpinsclinical research in rare diseases worldwide.

What are Clinical Research Networks – and why do they matter?

Clinical Research Networks are structured collaborations of expert clinical sites, laboratories, patient organisations and other stakeholders that join forces to accelerate prevention, diagnosis, epidemiological studies, natural-history studies and clinical trials for rare and groups of rare diseases.

By pooling scarce patient populations, harmonising protocols and sharing high-quality data, CRNs overcome the fragmentation that has long slowed progress in the field.Key themes on the agenda include:

  • Global efforts to advanceReal World Evidence (RWE) and data collection
  • Emerging technologies in diagnostics, prevention & clinical research
  • Lessons learned fromLow- and Middle-Income Countries (LMICs)
  • Medical Devices in trials for QoL, movements, evaluation
  • Strategies for effectivemulti-stakeholder engagement
  • The critical role ofpatients and partnerships in enabling international research access
  • Models of care andglobal research networks across income settings

As the rare disease community operates across borders, the need for inclusive, coordinated, and sustainable research networks is more pressing than ever. This conference provides a unique platform to exploresolutions that have a global impact yet are locally actionable.

Whether you conduct research, influence policy, or represent a patient’s voice, this event foresees two days of rich discussions, practical knowledge exchange, and meaningful connections. By sharing best practices, its aim is to foster mutual understanding of Clinical Research Networks (CRNs), strengthen its resources, and identify concretepathways to enhance collaboration and interoperability worldwide.

Event details

Date: 9–10 December 2025
Format: Hybrid – online and in-person participation available
Registration: here.
Further information: Programme details, speakers, and registration will be announced shortly.

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At the European Human Genetics Conference 2026 in Gothenburg, ERDERA’s Diagnostic Research Workstream reviewed progress, highlighted early results and used a major European genetics meeting to examine how advances in data sharing and genomic analysis may strengthen rare disease diagnosis across countries.
Boston, 9–11 June 2026: ERDERA's Scientific Coordinator joined the World Orphan Drug Congress USA to set out how stronger clinical research networks can make rare disease trials more feasible across sites and borders.
On 3–4 June, EURORDIS–Rare Diseases Europe and Orphanet convened the rare disease community at ECRD 2026 in Prague around a shared call for coordinated European action, including the forthcoming European Blueprint for Rare Diseases.