EURORDIS - The Voice of Rare Disease Patients in Europe

EURORDIS - The Voice of Rare Disease Patients in Europe



The Voice of Rare Disease
Patients in Europe



PATIENTS, ORGANISATIONS, SERVICES

See the EURORDIS COVID-19 Information Resource Centre, including our latest statements

COVID-19 Information Resource Centre

Please find below EURORDIS statements, sources of official information, and information/ activities organised in response to the pandemic that we have received through our network.

If you have any updates from the rare disease community on how your organisations are responding to the COVID-19 crisis please contact: davor.duboka@eurordis.org.

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