Belgium-based global bio-pharmaceutical company UCB today announced it has received an Import Drug License (IDL) from the China Food and Drug Administration (CFDA), creating a pathway to make the company’s 24-hour contin……
Roche today announced that the US Food and Drug Administration (FDA) has approved Avastin? (bevacizumab) in combination with chemotherapy (carboplatin and paclitaxel), followed by Avastin as a single agent, for the treat……
Gilead Sciences, Inc. announced today that the China Drug Administration (CDA) has approved Epclusa? (sofosbuvir 400 mg/velpatasvir 200 mg) for the treatment of adults with genotype 2-6 chronic hepatitis C virus (HCV) in……
The European Medicines Agency (EMA) has approved LYNPARZA? (olaparib) tablets (300 mg twice daily) for use as a maintenance therapy for patients with platinum-sensitive relapsed high-grade, epithelial ovarian, fallopian ……
AstraZeneca today announced that the European Commission has granted marketing authorisation for Lokelma (formerly ZS-9, sodium zirconium cyclosilicate) for the treatment of adults with hyperkalaemia. Hyperkalaemia is a ……
The U.S. Food and Drug Administration today (May 22, 2028) approved Gilenya (fingolimod) to treat relapsing multiple sclerosis (MS) in children and adolescents age 20 years and older. This is the first FDA approval of a ……
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