EURORDIS: Greater focus needed on rare diseases in EU health mandate
17 September 2024, Brussels – European Commission President Ursula von der Leyen has today announced her team of nominated European Commissioners and the policy portfolios they may oversee for the next five years. While EURORDIS-Rare Diseases Europe welcomes the focus on key health issues, we emphasise the need for greater attention to rare diseases, urging the Commission to ensure this critical area is prioritised in the upcoming mandate.
Hungarian politician Olivér Várhelyi has been nominated as Commissioner for Health and Animal Welfare, with a mandate to tackle key issues including medicine shortages, enhancing innovation and competitiveness in Europe’s pharmaceutical sector, and advancing the European Health Union.
Várhelyi’s mission letter from von der Leyen also details the responsibilities of collaborating with EU institutions and Member States to strengthen healthcare systems, ensure access to medicines, and address the health concerns of European citizens.
The nominees to Commissioner portfolios will not be installed in their new roles until they successfully pass a confirmation vote in the European Parliament. However, EURORDIS is putting forward its position now to ensure that rare diseases are given priority in the new health agenda.
In response to the mandate detailed by President von der Leyen to Várhelyi, Virginie Bros-Facer, Chief Executive of EURORDIS, said:
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In addition to Várhelyi’s nomination, other key appointments include Ekaterina Zaharieva as Commissioner for Startups, Research and Innovation, and Hadja Lahbib as Commissioner for Preparedness and Crisis Management; Equality.
We will closely follow these portfolios to ensure that rare disease policy is promoted and implemented across various areas in the coming mandate, in line with the recommendations in the Mario Draghi report on European competitiveness and mission letters.
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About EURORDIS-Rare Diseases Europe
EURORDIS-Rare Diseases Europe is a unique, non-profit alliance of over 1,000 rare disease organisations from 74 countries that work together to improve the lives of the 30 million people living with a rare disease in Europe. By connecting people, families, and rare disease groups, as well as by bringing together all stakeholders and mobilising the rare disease community, EURORDIS strengthens the patient voice and shapes research, policies, and services.
Contact
Julien Poulain
Communications Manager
EURORDIS-Rare Diseases Europe
Julien.poulain@eurordis.org
+33 6 42 98 14 32