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Q&A: Families shouldn’t have to coordinate Sweden’s rare disease care https://www.politico.eu/sponsored-content/families-shouldnt-have-to-coordinate-swedens-rare-disease-care/?utm_source=RSS_Feed&utm_medium=RSS&utm_campaign=RSS_Syndication #Advancedtherapies #Regions/Cohesion #Accountability #Communications #Healthsystems #Rarediseases #Transparency #Governance #Healthcare #Regulation #HealthCare #Hospitals #Medicines #Stability #Advocacy #Patients #Research #Services #Borders #Bridges #digital
Q&A: Families shouldn’t have to coordinate Sweden’s rare disease care

A Q&A with Zozan Sewger Kvist, CEO of rare disease competence center Ågrenska, on stalled reform, uneven access to care in Europe and the limits of regulation.

POLITICO
Mar 3 at 4:01amWeb