NEWS: Yann Le Cam of EURORDIS-Rare Diseases Europe on ECRD2020 – Register now https://youtu.be/00iYEfXxVLM The European Conference on Rare Diseases & Orphan Products (ECRD) is an unrivalled opportunity to network and exchange invaluable knowledge with all stakeholders in the rare disease Read More
NEWS: Industry attendance at ECRD2020 – Who should register? The European Conference on Rare Diseases & Orphan Products (ECRD) is an opportunity for industry to come together with patients to discuss the state-of-the-art in rare disease policy, research, diagnosis, treatment Read More
NEWS: Watch recording of #ECRD2020 pre-conference webinar The pre-conference webinar took place on Thursday 23 April. It was an opportunity to hear the latest outcomes of the Rare2030 Foresight Study and understand how the study lays a foundation for policy Read More
NEWS: Policymakers at ECRD2020 – Why Register? The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led rare disease event. Policymakers attending #ECRD2020 will join 1000+ other attendees from around the world (including patient advocates, healthcare Read More
NEWS: Latest set of speakers announced for world largest patient led rare disease conference ECRD2020 – Register Now We are delighted to announce the first set of speakers for European Conference on Rare Diseases & Orphan Products (ECRD) 2020. #ECRD2020 Read More
NEWS: Clinicians at ECRD2020 – Why Register? The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led rare disease event. Clinicians attending #ECRD2020 will join 1000+ other attendees from around the world (including patient advocates, healthcare Read More
NEWS: Patients at ECRD2020 – Why Register? The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led rare disease event. Patients attending #ECRD2020 will join 1000+ other attendees from around the world (including patient advocates, healthcare Read More