EURORDIS - The Voice of Rare Disease Patients in Europe

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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



Breaking the Access Deadlock to Leave No One Behind



      A contribution by EURORDIS and its members on possibilities for patients' full and equitable access to rare disease therapies in Europe

      EURORDIS Position Paper Breaking the Access Deadlock
      This position paper is a contribution from EURORDIS and its members that offers a synthesis of their analysis, reflections and perspectives on the issue of access to rare disease therapies.
      The position paper sets out a new four-pillar approach to tackling the challenges that prevent patients’ access to care and medicines, as well as the ambition to have 3 to 5 times more new rare disease therapies approved per year by 2025, 3 to 5 times cheaper than today.
      In the paper, EURORDIS calls for a new model based on a collective conversation involving all stakeholders (patients, the pharmaceutical industry, national competent authorities, national health ministries, researchers, scientists and the European Medicines Agency).


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