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- What is an orphan drug?
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- Role of EURORDIS
- Patient advocates involvement
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- Health technology assessment
- EURORDIS Round Table of Companies (ERTC)
- List of the latest marketing authorisations and orphan medicinal products designations
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All EURORDIS Training Modules have been licensed with Creative Commons. The modules can be used for non commercial purposes only providing that EURORDIS is sited as the author.
The EURORDIS Training Modules are registered with Attribution-Noncommercial-ShareAlike 3.0 license from Creative Commons
Statistics Module: 
EURORDIS e-learning module Statistics by EURORDIS is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
Ethics Module: 
EURORDIS Training Module on ETHICS by EURORDIS is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
Methodology Module:
EURORDIS Training Module on METHODOLOGY by EURORDIS is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
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The voice of rare disease patients in Europe
The international voice of people living with rare diseases, Rare Diseases International is a EURORDIS initiative
Bringing together patients, families and experts to share experiences in a moderated multi-language forum.
The Rare Barometer Programme is a EURORDIS initiative that carries out surveys to transform rare disease patients' experiences into figures and facts that can be shared with decision-makers.
An international awareness raising campaign taking place on the last day of February each year, Rare Disease Day is a EURORDIS initiative
Join the largest gathering of rare disease stakeholders across Europe, at the biennial European Conference on Rare Diseases and Orphan Products. ECRD is a EURORDIS initiative
The international voice of people living with rare diseases, Rare Diseases International is a EURORDIS initiative
Bringing together patients, families and experts to share experiences in a moderated multi-language forum.
The Rare Barometer Programme is a EURORDIS initiative that carries out surveys to transform rare disease patients' experiences into figures and facts that can be shared with decision-makers.
An international awareness raising campaign taking place on the last day of February each year, Rare Disease Day is a EURORDIS initiative
Join the largest gathering of rare disease stakeholders across Europe, at the biennial European Conference on Rare Diseases and Orphan Products. ECRD is a EURORDIS initiative