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EMA approves Biocon Biologics’ new mAbs facility in India

European Medicines Agency also renews GMP certifications for Biocon's manufacturing sites in India and Malaysia, enhancing global biosimilars supply

GSK’s Arexvy label expansion will intensify competition with Pfizer’s Abrysvo in...

The European Medicines Agency (EMA) recently accepted the company’s regulatory application to expand the use of Arexvy and a decision is anticipated in H2 2024

Takeda launches drug for treating hereditary angioedema patients in India

CINRYZE™ is plasma-derived C1-I NH approved for routine prevention (prophylaxis), short-term prevention or pre-procedure prevention, and acute attacks of HAE