Summary of Rare Disease Activities in Sweden*

(Full report accessible below)

Full 2016 report on Rare Disease Activities in Sweden

*NB – The findings and conclusions in this report are those of the contributors and validating authorities, who are responsible for the contents; the findings and conclusions do not necessarily represent the views of the European Commission or national health authorities in Europe. Therefore, no statement in this report should be construed as an official position of the European Commission or a national health authority.

Information supplied by the Swedish SOA Data Contributing Committee:

• Competent National Authority – Jonas Bergström
• Orphanet National Representative – Désirée Gavhed
• National Patient Alliance Representatives – Elisabeth Wallenius and Raoul Dammert