CDSCO Panel Demands Structured Phase IV Protocol for Ademetionine in Liver Disease Subtypes Dr. Divya Colin15 May 2025 6:00 PM ISTNew Delhi: After reviewing the Phase IV clinical trial report of Ademetionine Tablets, the Subject Expert Committee (SEC) functioning under the...
Mankind Pharma hit with over Rs 341 crore additional tax demand from IT authority Ruchika Sharma15 May 2025 5:41 PM ISTNew Delhi: Mankind Pharma Limited has disclosed the receipt of orders from the IT Authority, raising additional tax demands (including interest) of Rs...
GSK to acquire liver disease drug Efimosfermin for up to USD 2 billion Ruchika Sharma15 May 2025 4:10 PM ISTLondon: GSK plc and Boston Pharmaceuticals, a clinical stage biopharmaceutical company developing highly targeted therapies for patients with...
USFDA clears Alembic Pharma cardio drug Rivaroxaban, launch expected in next year Ruchika Sharma15 May 2025 3:26 PM ISTVadodara: Alembic Pharmaceuticals Limited has announced that it has received final approval from the US Food & Drug Administration (USFDA)...
USFDA issues EIR for Zydus Lifesciences Ambernath facility Ruchika Sharma15 May 2025 1:45 PM ISTAhmedabad: Zydus Lifesciences has announced that the company has received the Establishment Inspection Report (EIR) report from...
After Baclofen, now Gabapentin: Marksans Pharma arm bags another UK MHRA green light Ruchika Sharma15 May 2025 12:56 PM ISTMumbai: Marksans Pharma Limited has announced that its wholly owned subsidiary in the UK, Relonchem Limited, has received Marketing...
Merck scores USFDA OK for Welireg for 12 years and older with pheochromocytoma or paraganglioma Ruchika Sharma15 May 2025 11:45 AM ISTRahway: Merck, known as MSD outside of the United States and Canada, has received the approval from the U.S. Food and Drug Administration...
AbbVie Emrelis gets USFDA accelerated approval for a type of lung cancer Ruchika Sharma15 May 2025 11:10 AM ISTNorth Chicago: AbbVie has received accelerated approval from the U.S. Food and Drug Administration (FDA) for EMRELIS (telisotuzumab...
Shilpa Pharma Lifesciences Unit 1 gets EIR from USFDA Ruchika Sharma15 May 2025 10:15 AM ISTKarnataka: Shilpa Pharma Lifesciences, a 100% subsidiary of Shilpa Medicare Limited, has received an Establishment Inspection Report...
Andhra Pradesh CM unveils Bharat Biotech arm Lumpy Skin Disease vaccine Ruchika Sharma14 May 2025 6:01 PM ISTVijayawada: Chief Minister of Andhra Pradesh Shri N. Chandrababu Naidu has launched the indigenous Lumpy Skin Disease (LSD) vaccine BIOLUMPIVAXIN,...
Unichem Labs Pithampur facility gets USFDA EIR Ruchika Sharma14 May 2025 5:39 PM ISTMumbai: Unichem Labs has announced that United States Food and Drug Administration (USFDA) has classified the inspection at the Company's...
USFDA nod to generic therapeutic equivalent version of Janssen Pharma Haldol injection Ruchika Sharma14 May 2025 3:38 PM ISTChennai: Caplin Steriles Limited, a Subsidiary Company of Caplin Point Laboratories Limited, has received final approval from the...
