IRDiRC is an associate partner of the ECRD.
The event 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.
The event draws together more than 800 participants from over 50 countries around the world. Leading, inspiring and engaging all stakeholders to take action, ECRD is where innovative solutions in the rare disease field are born. 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.
15 – 16 May 2020. Stockholm, Sweden.
Program is available for consultation.
Early bird registration is open until 20 March 2020.
Submissions for poster abstracts are now open until 10th February 2020.
Applications for the Patient Advocate Fellowship Programme are now open until 2 December 2019.