Drug Approval | November 13, 2024
EMA grants GMP Certificate of compliance to CuraTeQ biosimilars’ Hyderabad facility
The GMP inspection assessed mammalian and microbial drug substance manufacturing facility sections
The GMP inspection assessed mammalian and microbial drug substance manufacturing facility sections
The inspection concluded with the issuance of Form 483 with four observations which are procedural in nature
This is used to treat central diabetes insipidus and bedwetting
Critical resources will help Genvor to grow and scale biological crop protection products and innovative trait technologies
Kwality Pharma already has registration of 20 molecules from the units and 20 are under registration
GL0034 administered once-weekly confirmed clinically meaningful weight loss and improved glucometabolic parameters over a 4-week treatment period in individuals with obesity
Zealand Pharma anticipates initiation of a Phase 2b clinical trial in H2 2024
This is the first peptide product approval from the USFDA received by Alembic Pharmaceuticals
Establishing Asymchem’s first manufacturing footprint in Europe
EBITDA for the quarter stood at Rs 964 crore, representing an EBITDA margin of 24%
Subscribe To Our Newsletter & Stay Updated
