Abstract
EUROPLAN is an operational measure within the European strategy in the field of RD. The project aims at a) elaborating recommendations on the different steps to develop a national plan or strategy; they will include priority areas and actions of intervention supporting the harmonisation of public health strategies on RD throughout Europe; b) select indicators for monitoring the implementation and evaluating the impact of national plans or strategies. In order to turn the Council Recommendation into concrete actions in favour of RD patients at national level, several rare disease patient alliances, coordinated by EURORDIS in conjunction with national authorities, are organising National Conferences to be held in 16 Countries in 2010. During the National Conferences local stakeholders will discuss the EUROPLAN recommendations and the main elements of the European strategy on RD, with the aim to assess their transferabil-ity in their own Country. In conclusion, EUROPLAN is collecting information on EU Member States initiatives contributing to share experiences, data and effective strategies to address RD; is promoting the development of RD plan or strategy trough recommendations and indicators; is increasing awareness on RD and the recommendations will also serve as an important advocacy instrument at policy level. The EUROPLAN outcomes will support and encourage EU MS in developing national health policies to ensure equal access and availability of prevention, diagnosis and treatment for citizens with RD.
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CITATION STYLE
Taruscio, D., & Vittozzi, L. (2010). European Project for Rare Diseases National Plans Development (EUROPLAN). Orphanet Journal of Rare Diseases, 5(S1). https://doi.org/10.1186/1750-1172-5-s1-p2
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