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A paper on a Charitable Access Program for patients with lysosomal storage disorders in underserved communities worldwide has now been published online on the Orphanet Journal of Rare Diseases (OJRD) website.
IGA's CEO, Tanya Collin-Histed says "We are delighted to share this publication with you. The IGA has been a part of this programme now for 10 years as a member of the Medical Expert Committee (MEC).