News- EIKRA

IRDiRC Announces New Leadership for the Therapies Scientific Committee

The International Rare Diseases Research Consortium (IRDiRC) is pleased to announce the appointment of Shekhar Natarajan (Vice President, Head of EU and International Regulatory Affairs at Dyne Therapeutics, USA), as Chair, and Diana Kwast-Hoekstra (Executive Director at (Un)limited Forward!, Netherlands), as Vice Chair of the Therapies Scientific Committee (TSC). The TSC unites a diverse group of stakeholders from across the global […]

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Four weeks to go: register now for the 2nd International Conference on Clinical Research Networks

With less than one month to go, registrations are still open for the 2nd International Conference on Clinical Research Networks — a two‑day hybrid meeting designed to align global efforts on data, diagnostics and trials for rare diseases.  The conference is organised by the European Rare Diseases Research Alliance (ERDERA), the International Rare Diseases Research Consortium (IRDiRC) […]

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Showcase Your Work at ECRD 2026 — Europe’s Largest Rare Disease Event

Are you advancing research, shaping policy, or driving advocacy for people living with rare diseases? Share your work with Europe’s rare disease community at the European Conference on Rare Diseases & Orphan Products (ECRD 2026) — Europe’s largest, patient-led rare disease event organized by EURORDIS Rare Disease Europe, taking place on 3–4 June 2026 in Prague, Czech Republic. […]

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Highlights from the World Orphan Drug Congress 2025

The World Orphan Drug Congress 2025 brought together leading voices in the rare disease community for 3 days of insight, collaboration, and forward-looking discussion. Representatives from the International Rare Diseases Research Consortium (IRDiRC) shared key perspectives on advancing research and improving access to therapies for people living with rare conditions. A highlight of the congress, which took place […]

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New IRDiRC Publication: “What Matters Ethically About How the UDN Has Changed Since Its Inception”

IRDiRC is pleased to share a new publication “What Matters Ethically About How the UDN Has Changed Since Its Inception”, recently published in AMA Journal of Ethics. For individuals living with undiagnosed rare diseases, the search for a diagnosis can be long, uncertain, and emotionally burdensome. A delayed diagnosis, or none at all, can significantly add […]

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New IRDiRC Publication: “Applying the international rare disease research consortium (IRDiRC) N-of-1 therapy task force eligibility criteria for individualised therapies use case: Duchenne muscular dystrophy”

IRDiRC announces publication of a new manuscript, developed as part of the International Rare Disease Research Consortium (IRDiRC) N-of-1 Task Force: “Applying the IRDiRC N-of-1 Therapy Task Force Eligibility Criteria for Individualised Therapies – Use Case: Duchenne Muscular Dystrophy“. Nucleic acid-based therapies, including antisense oligonucleotides (ASOs), are opening new doors for the treatment of rare diseases. With over […]

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From discussion to action: a hands‑on conference to help shape the rare disease clinical research roadmap

The 2nd International Conference on Clinical Research Networks for Rare Diseases will take place on 9–10 December 2025 in Heidelberg, Germany, with full hybrid access for participants worldwide. This edition features a distinctly hands-on format, placing delivery at the centre. Each session —plenary and workshops alike— will close with agreed action points that will be captured live […]

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IRDiRC at World Orphan Drug Congress Europe 2025

The International Rare Diseases Research Consortium (IRDiRC) is pleased to participate in this year’s World Orphan Drug Congress Europe, taking place from 27–29 October 2025 in Amsterdam, Netherlands. We warmly invite all attendees to visit the IRDiRC booth (10.510) to learn more about our mission, collaborative initiatives, and how we are accelerating the development of diagnostics and therapies for people living with […]

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New webinar: “Genetics and unique populations: The Case of the Finnish, Roma and Irish Travellers”

Professor Sally Ann Lynch, chair of IRDiRC Diagnostics Scientific Committee (DSC), will be chairing the upcoming ERN ITHACA webinar on “Genetics and unique populations: The Case of the Finnish, Roma and Irish Travellers”.With a deep expertise in rare diseases, endogamous populations and clinical risk, Professor Lynch will discuss about different barriers in healthcare access across […]

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