The Rare Disease Action Forum
Improving Access to Diagnosis, Treatment and Care for Patients with Rare Diseases
Who we are
The RDAF is a unique, multi-stakeholder organization in the field of rare diseases in Switzerland. Established in Switzerland, the RDAF is not-for-profit organization that aims to increase awareness about rare diseases and adaptations of the Swiss regulatory framework to improve patients’ access to diagnosis, treatment and care.
Our mission
Raise awareness about the challenges the rare disease community faces
Shape the regulatory framework in the field of rare diseases in Switzerland
Enable equal and fair access to diagnosis, treatment and care for patients with rare diseases
United action
RDAF activities
Check out our brochure to learn more about the RDAF and its activities.
