RARE DISEASES INTERNATIONAL
SAVE THE DATE
Rare Diseases International Policy Event
The Right to Health: The Rare Disease Perspective
10 February 2017, 10.00 – 17.00, 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 those with rare diseases’
Helen Clark, Administrator of the UN Development Programme
To mark the occasion of Rare Disease Day 2017, Rare Diseases International, the Global Alliance of Rare Disease Patients, in partnership with the BLACKSWAN Foundation, the Swiss Foundation for Research on Orphan Diseases, and EURORDIS-Rare Diseases Europe, invite you to join people living with a rare disease and policy makers at a unique face-to-face discussion.
The event is the first of its kind to be organised in Geneva and will gather international experts in the fields of public health, human rights, epidemiology, scientific research and patient advocacy to discuss why and how rare diseases should be included in the global health agenda.
After registering you will receive a confirmation email. Please be aware that places are limited – you will need to receive confirmation in order to attend.
There is no registration fee for this event. Please be advised that accommodation and travel expenses are not covered by the organisers.
There is no registration fee for this event. Please be advised that accommodation and travel expenses are not covered by the organisers.
This is an event in partnership and with support from the BLACKSWAN Foundation and EURORDIS, with the participation of IRDiRC, the NGO Committee for Rare Diseases, and Orphanet.
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