The ECRD is recognised globally as the largest, patient-led rare disease event. People living with a rare disease have the right to reach their highest potential of well-being; join the ECRD 2020 Stockholm to take part in discussions to inform and build the future ecosystem for rare disease policies and services. 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 from over 50 countries around the world - Patient representatives, policy makers, researchers, clinicians, industry representatives, payers and regulators.
Be part of the global rare disease community at ECRD 2020 Stockholm and shape the future for people living with a rare disease!
NOW OPEN - Application for Patient Advocate Fellowships (Deadline: 2nd December 2019) APPLY HERE
NOW OPEN - Poster Abstract Submission (Deadline: 10th February 2020) SUBMIT YOUR ABSTRACT HERE
Registration will open in the second half of November!
For more Information, please visit the the official ECRD Website www.rare-diseases.eu.