REPLAGAL 1 MG/ML PERF FL 3,5 ML
(Agalsidase Alfa) - Maladie rare sans désignation orpheline
Long-term enzyme replacement therapy in patients with a confirmed diagnosis of Fabry Disease (alpha-galactosidase A deficiency)
Business Listing - September 18, 2019
This is a premium business listing. Stand out from the competition!