jueves, 16 de abril de 2020

EURORDIS - The Voice of Rare Disease Patients in Europe

EURORDIS - The Voice of Rare Disease Patients in Europe

Eurordis, Rare Diseases Europe

The Voice of Rare Disease
Patients in Europe



PATIENTS, ORGANISATIONS, SERVICES


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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