This office will be the central hub for all operations related to companies ethical pharmaceutical business
Doses will be ready to ship to applicable European Union (EU) member states as soon as possible upon European Commission (EC) authorization
Glenmark Pharmaceuticals Limited has informed that the USFDA has issued Form 483 with zero observations
Stable profits, low leverage to keep credit profiles comfortable
USFDA concludes inspection of Dr. Reddy's Laboratories R&D centre in Bachupally with zero observation
Takeda has granted Lupin non-exclusive patent licensing rights to commercialize Vonoprazan in India
Tecentriq Hybreza provides patients and physicians with greater flexibility of treatment options while showing safety and efficacy consistent with intravenous
The sANDA was submitted as “Prior Approval Supplement” for addition of an alternate drug product manufacturing, labeling, packaging, and testing facility
Investment in new plant meets increasing demand for functional excipients for oral drug delivery
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