USFDA completes inspection of Lupin's Dabhasa facility with no observations
The inspection was conducted from April 8 to April 12, 2024 and concluded with no observations
The inspection was conducted from April 8 to April 12, 2024 and concluded with no observations
The partners will collaborate to build a cutting-edge oligonucleotide cGMP manufacturing facility
These observations are procedural in nature and will be responded within the stipulated time
Asahi Songwon Colors' shareholding in ALSPL has increased from 78% to 100%
The approved product has an estimated market size of US$ 44.5 million for the twelve months ending January 2024
Contributing to lower risk of potentially carcinogenic nitrosamine impurities in pharmaceuticals
Shivalik Rasayan Limited have successfully submitted USMDF for API " Palbociclib " to USFDA
The bioprocess business will continue to pioneer contributions to safety and productivity in the manufacture of biotherapeutics
The product is an additional formulation of Cresemba Capsule 100 mg and Cresemba Intravenous Infusion 200 mg
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