Förderverein für Kinder mit seltenen Krankheiten (KMSK) joins Rare Disease Action Forum

    3 May, 2024

    We are happy to welcome Förderverein für Kinder mit seltenen Krankheiten (KMSK) as the newest member of the Rare Disease Action Forum (RDAF). With Förderverein für Kinder mit seltenen Krankheiten (KMSK) on board, RDAF’s diverse coalition gains further strength, complementing the participation of industry partners, patient organizations, healthcare professionals, and research institutions.

    We eagerly anticipate the significant contributions Förderverein für Kinder mit seltenen Krankheiten (KMSK) will bring to the collaborative efforts within the RDAF framework. Together, we stand resolute in our commitment to improving access to diagnosis, treatment, and care for individuals affected by rare diseases in Switzerland.

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    RDAF hosts Swiss Rare Disease Summit on 26 November 2024

    The Rare Disease Action Forum (RDAF) will host the Swiss Rare Disease Summit on 26 November 2024 (9.30 – 17.30 CEST). The event will take place in Bern, with the additional option of virtual attendance. The Swiss Rare Disease Summit endeavors to forge a collective...