ZVEZA EUROPSO

EUROPSO is a patient umbrella organisation with an overall goal to achieve better conditions for early diagnostics, access to treatment and improving the quality of life for all patients suffering from psoriasis in Europe. In order to achieve this goal, EUROPSO organises activities to educate and raise awareness of this condition, helping social and economic integration of psoriasis/psoriasis arthritis patients and dispelling prejudices and all other forms of discrimination against psoriasis/psoriasis arthritis patients.
EUROPSO works with other organisations which share the same or similar goal. In order to reach a wider group of decision makers on the EU level, one of EUROPSO’s aims is obtaining recognition from the European Union and other European international institutions.

We operate in the health sector for the better recognition of psoriasis and arthritis psoriasis within the existing health policies. EUROPSO activities are aimed at protecting the rights of patients, to ensure equal access to treatment and the right therapeutic path.

EUROPSO would like to represent the psoriasis patient voice within the “EU4Health Programme” (the Regulation (EU) 2021/522 of the European Parliament and of the Council of 24 March 2021 establishing a Programme for the Union’s action in the field of health (‘EU4Health Programme’) for the period 2021-2027, and repealing Regulation (EU) No 282/2014 (Text with EEA relevance)).

www.euro-pso.org

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No lobbyists with EP accreditations

EUROPSO did not participated in any of the aforementioned EU-level activities until now.
All EUROPSO related work is being carried out by volunteers, members of the Board.

Data not provided by Register Secretariat due to GDPR

Data not provided by Register Secretariat due to GDPR

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