Lupin completes successful Phase 3 trials for Lucentis biosimilar
The successful completion of the global Phase 3 trials paves the way to obtain marketing approval in the U.S. and EU
The successful completion of the global Phase 3 trials paves the way to obtain marketing approval in the U.S. and EU
Dr. Reddy's had previously received the EU GMP certificate for its Rituximab drug substance
The approval of YESAFILI marks Biocon Biologics’ expansion into the ophthalmology therapeutic area in the United States
Sun Pharma's Dadra facility receives OAI status from US FDA
Project achieves 30% reduction in hospital acquired infections and 24% reduction in the incidence of multi-drug resistant organisms
The agreement is effective from January 1, 2024 and commercialisation commenced on February 1, 2024
Trastuzumab biosimilar is a humanized monoclonal antibody for treating metastatic breast cancer
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