European Registries for Rare Endocrine and Bone Conditions
Research
→Research
Use e-REC to easily capture new clinical encounters, or use the Core Registry for in-depth, long-term patient data collection and research, with common data elements and condition-specific modules.
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Quick Links
Europe’s Resource for Rare Endocrine and Bone Conditions
EuRREB supports healthcare professionals, researchers, and patients in collecting data through patient-centered registries and enabling collaborative research across Europe to improve care for those affected by rare endocrine and bone diseases.
Upcoming events
Together, we advance care for rare diseasesImproving knowledge||Accelerating research||Empowering patients||Shaping better policies||Transforming lives
Improving knowledge
||Accelerating research
||Empowering patients
||Shaping better policies
||Transforming lives
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participating centres
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new patients seen by a centre
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cases with detailed information
reported by clinicians and patients
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Mar
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2025
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2024
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12
2024
