The Swiss Rare Disease Summit brings together patients, healthcare professionals, researchers, policymakers, regulatory authorities and industry leaders to advance the future of rare disease policy, care and innovation in Switzerland. The programme addresses evidence and access, transition, patient involvement, diagnostic pathways, regulatory and health-policy frameworks, and international collaboration. Join this multi-stakeholder dialogue at Kinderspital Zürich. Participation is free of charge.
Hosted by
- Rare Disease Action Forum (RDAF)