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            Rare Diseases International Policy Event The Right to Health: The Rare Disease Perspective 10 February 2017, 09.30 – 18.00, Campus Biotech, Chemin des Mines 9, 1202 Geneva, Switzerland   ‘No country can claim to have achieved universal healthcare if it has not adequately and equitably met the needs of […]

10 February 2017, Geneva – A-first-of-its-kind event takes place today in Geneva to bring together international experts in the fields of public health, human rights, scientific research, patient advocacy and the health industry to discuss why and how rare diseases should be part of the global health agenda.

EURORDIS-Rare Diseases Europe has recently established a partnership with the Rare Disease Foundation of Iran, a non-profit and non-governmental institution that provides services for rare disease patients and their community in Iran.

The Rare Diseases Conference that took place in October 2016 provided a global forum for all stakeholders within the rare diseases field to participate in open discussion, enhance models of best practice and share specialist knowledge around rare diseases and orphan drugs.

ICORD is very pleased to announce this statement on rare diseases and the development agenda, presented by Helen Clark, Administrator of the United Nations Development Programme.

RDI’s Annual Meeting was held on May 25th, 2016 – the day before and in the same premises as the European Conference on Rare Diseases & Orphan Products (ECRD 2016) in Edinburgh, Scotland.

The first annual meeting of RDI took place in May 28, 2015 in Madrid, Spain, alongside the EURORDIS Membership Meeting. Over 60 patient representatives from 30 countries gathered for the official launch and inaugural meeting.