Healthcare Industry at ECRD2022 – Why Register? The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led rare disease event. Industry representatives attending #ECRD2022 joined 1000+ other attendees from around the world (including peers, patient advocates, Read More
Policy makers at ECRD2022 – Why Register? The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led rare disease policy event. Policy makers attending #ECRD2022 joined 1000+ other attendees from around the world (including peers, patient Read More
Topics presented during the conference To help participants navigate the conference, the visual below details the main topics included in the programme. The icons related to each topic appear on the Programme at a Glance in each of the sessions Read More
Healthcare professionals at ECRD2022 – Why Register? The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led rare disease healthcare event. Healthcare professionals attending #ECRD2022 joined 1000+ other attendees from around the world (including peers, patient Read More
Poster Contest Winners Congratulation to all authors for your amazing work! Out of the over 250 high-quality posters we have received for ECRD 2022, we are delighted to present to you the four top scoring ones, listed below, which were Read More
Patients at ECRD2022 – Why Register? The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led rare disease event. Patients attending #ECRD2022 joined 1000+ other attendees from around the world (including fellow patient advocates, healthcare professionals, Read More
Meet our exceptional chairs ECRD 2022 was the opportunity to meet our session chairs from around the world who were be taking part in the ECRD 2022 conference. To help us create the ecosystem required to address the unmet needs Read More
Continuing Education ECRD 2022- Register Now Thanks to the expertise of over 100 expert speakers, ECRD 2022 has once again been approved by the Commission for Professional Development (CPD) of the Swiss Association of Pharmaceutical Professionals (SwAPP) and the Swiss Read More
Satellite Meetings Recognised globally as the largest, patient-led rare disease policy event, the ECRD is a unique opportunity to gather key opinion decision makers in various countries to consider how EU policies and national strategies will link in the coming Read More
Thought Leader Sessions For this year’s ECRD, participants had the opportunity to join 3 innovative Thought Leader Sessions to learn more about Together4RD (Multi-stakeholder initiative to unlock European Reference Networks (ERN) collaboration with industry), Rare Diseases International – Preparing the foundations Read More