Caplin Point announces completion of unannounced USFDA inspection
The inspection was concluded with zero observations
The inspection was concluded with zero observations
Against targeted investment of Rs. 3,938 crore, investments worth Rs. 4,024 crores have been made under scheme
Organization to provide vaccinations & treatments for several monsoon related diseases and illnesses across all 102 clinics
The successful completion of the global Phase 3 trials paves the way to obtain marketing approval in the U.S. and EU
Emraclidine, a potential best-in-class, next-generation antipsychotic, is in trials designed to be registration enabling for schizophrenia
More emphasis should be given on investing healthcare resources towards prevention of diseases rather than only focusing on diagnostic and therapeutic options
Dr. Reddy's had previously received the EU GMP certificate for its Rituximab drug substance
Decision on EU marketing authorisation for this population expected by September 2024
The inspection scope included 6 separate Biologics manufacturing units comprising 4 Drug Substance and 2 Drug Product manufacturing plants
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