Jan 18 2012
Genzyme, a Sanofi company (EURONEXT: SAN and NYSE: SNY), announced today that the European Medicines Agency (EMA) has approved its manufacturing plant in Framingham, Mass., for the production of Fabrazyme® (agalsidase beta).
"This approval by the EMA represents an important milestone in our manufacturing recovery and path toward unconstrained supply for all patients," said Genzyme's President and CEO David Meeker. "Providing the Fabry community with consistent access to treatment, increasing our inventory of Fabrazyme® and working toward all regulatory approvals of our Framingham plant are our highest priorities, and we remain on track to achieve all of these crucial goals."
Canada’s proactive policies reduce drug shortages far more effectively than the U.S.