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CDSCO Launches Online Risk Classification Module for Non-IVD Medical DevicesIndian medical devices share increased from 10% to 30% of domestic requirements in last 5 years: DoP...
AstraZeneca-Daiichi Sankyo Enhertu gets USFDA Breakthrough Therapy Designation in HER2-positive early breast cancerAstraZeneca announces Rs 176 crore investments in India to expand Chennai GITC
Eli Lilly Jaypirca met its primary endpoint in head-to-head Phase 3 study versus ImbruvicaEli Lilly gets USFDA Breakthrough Therapy designation for olomorasib with Keytruda for lung cancer
NPPA Notifies New MRP for Key Cardiac, Diabetes and Antibiotic Drugs, DetailsNPPA fixes Special Ceiling Price for Gufic's Meropenem Dual Chamber Bags
Sun Pharma Asked to Resubmit Revised Phase III Protocol for Delafloxacin CABP TrialSun Pharma Fails to Secure CDSCO Nod for BE, Phase III Waiver on Sitagliptin, Glimepiride, Metformin...
Takeda announces closing of partnership with Innovent Biologics for oncology medicinesUSFDA approves expanded indication for Takeda Vonvendi for adults, children with Von Willebrand...
Roche Lunsumio VELO bags USFDA approval for subcutaneous use in follicular lymphomaRoche receives EU CE mark for Contivue for neovascular age-related macular degeneration
Drug Safety Alert: IPC Flags Adverse Reactions linked to Tranexamic acid and MetoclopramideDrug Safety Alert: IPC Flags Adverse Reactions linked to Tranexamic acid and Metoclopramide
Virchow Biotech gets CDSCO panel nod to study Semaglutide for chronic weight managementVirchow Biotech gets CDSCO panel nod to study Semaglutide for chronic weight management
Govt Amends Marketing Code for Medical Devices, DetailsGovt Amends Marketing Code for Medical Devices, Details
NMC Yet to Act against 30 Doctors for Sponsored Foreign TripsSC Questions Effectiveness of UCPMP, Seeks Govt Clarification on Pharma Freebies
Dr Reddys Labs secures European Commission approval for biosimilar to treat osteoporosisDr Reddy's Labs API Mirfield facility gets 7 USFDA observations
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