The ECRD is recognised globally as the largest, patient-led rare disease event in which collaborative dialogue, learning and conversation takes place, forming the groundwork to shape future rare disease policies.

Leading, inspiring and engaging all stakeholders to take action, the Conference is an unrivalled opportunity to network and exchange invaluable knowledge with all stakeholders in the rare disease community  – patient representatives, policy makers, researchers, clinicians, industry representatives, payers and regulators.

Join us at ECRD 2020 online to take part in discussions to inform and build the future ecosystem for rare disease policies and services.

DÉCOUVREZ

les dernières avancées, les enjeux, les faits, les chiffres et les tendances du domaine des maladies rares avec plus de 100 conférenciers experts.

FAÇONNEZ L’AVENIR

des maladies rares aux côtés des représentants de patients, de l’industrie pharmaceutique, d’un État membre ou d’un organisme de réglementation, des décideurs, des cliniciens et des payeurs.

RÉSEAUTEZ &
PRÉSENTEZ VOS TRAVAUX

à toutes les parties prenantes de la communauté maladies rares !

Shaping the future of health in the EU together is more urgent than ever. The #EU4Health coalition is urgently calling on @Europarl_EN @EU_Commission & @EUCouncil
to ACT NOW for a stronger health policy. Read/sign our joint statement: ... http://ow.ly/e4WI50zRlCH #StrongerTogether

Thank you to all patient representatives from Central & Eastern Europe countries who participated in a recent @imi_paradigm workshop to give feedback on tools being developed to support sustainable patient engagement in medicines R&D
Read more 👉 ... https://imi-paradigm.eu/cee-patient-engagement-conference-transferability-workshops-report/

We're looking for people affected by any of these #rarediseases that would like to connect with others living with the same condition. Interested? Send us an email at [email protected] or visit http://RareConnect.org

Share this image and help us ... #BreakTheIsolation!

Calling all #raredisease & rare cancer patient advocates
👉Register now for the first webinar of the EURORDIS Digital School 2020-2021 on the topic 'Helping Patient Organisations Plan and Create for Social Media Success' (18 June) ... https://us02web.zoom.us/meeting/register/tZYrdOyvqzstGNOl5aT2g96lcy4-CuI8l5kB
@castrorakel

Register now - EURORDIS will be co-hosting a webinar with @EU_Health of @EU_Commission on 9 June "The impact of #COVID19 for people living with a Rare Disease" during which we will present results from our COVID-19 survey by ERN disease grouping. Register: ... https://ec.europa.eu/health/sites/health/files/ern/docs/ev_20200609_ag_en.pdf

Organisé par :

Co-organisé par :

 

Avec le soutien de :

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Partenaires :

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Eucope logo
EuropaBio logo
HOPE logo
Rare2030 logo
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Partenaires associés :

Partenaires médias