European Conference on Rare Diseases & Orphan Products (ECRD)
In the context of the current COVID-19 pandemic, the upcoming European Conference on Rare Diseases & Orphan Products (ECRD) will take place ONLINE on 14-15 May (more information)
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.
Important note: ECRD 2020 will now take place ONLINE on 14-15 May -> more information
New registration categories and fees
|Delegate category||Registration Fees|
|EURORDIS members* patients’ organisations, all Swedish patients’ organisations and RDI members patients’ organisations||40 €|
|Non-EURORDIS members patients’ organisations||75 €|
|ERN representatives/ academics / healthcare professionals/ researchers||150 €|
|EURORDIS Round Table of Companies members**||980 €|
|Healthcare industry, consultants, investors||1225 €|
|Payer bodies/ HTA agencies/ national competent authorities/ regulators/ policy makers or government workers||Complimentary|
|Medical Students||40 €|
|Speakers at ECRD||Please do not use the button below, you have been/will be provided a specific registration link via email|
Media representatives -> Please contact Eva Bearryman, Senior Communications Manager, to request a press pass to join the conference online: eva.bearryman@
- Da 14 Maggio 2020 a 15 Maggio 2020
Powered by iCagenda