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Lilly’s Obesity Portfolio Wins Full U.S. Insurance Coverage, Reshaping the GLP-1 Landscape

In a pivotal shift for the obesity treatment market, Eli Lilly and Company (NYSE: LLY) has secured formulary coverage across all three of America's largest pharmacy benefit managers —...

Dabur India Plant Under US FDA Scanner Over Contamination Concerns

The United States Food and Drug Administration (US FDA) has flagged serious concerns at Dabur India's manufacturing facility...

FDA Approves Wockhardt’s Novel Antibiotic ZAYNICH™️ for cUTI

Wockhardt Limited  announced that the U.S. Food and Drug Administration (FDA) has approved ZAYNICH™ (cefepimeand zidebactam), a novel intravenous antibiotic...

Relief for Patients: NPPA Fixes Ceiling Prices for 30 Essential Medicines

The National Pharmaceutical Pricing Authority (NPPA) has notified ceiling prices for 30 essential fixed-dose combination medicines under the...

FDA Draft Guidance Aims to Reduce Animal Testing for Cancer Drugs

The U.S. Food and Drug Administration (FDA) issued a new draft guidance aimed at reducing unnecessary animal testing...

Union Health Ministry Accelerates Digital Maternal Healthcare with JANANI Platform Launch

The Union Health Ministry has launched the JANANI platform, a major digital healthcare initiative aimed at strengthening maternal and child healthcare services across India....

Zydus Fast-Tracks Malaria Fight: DCGI Greenlights Phase III Trials for Breakthrough Drug Zintrodiazine

Zydus Lifesciences Limited (“Zydus”), a leading innovation-driven global lifesciences company, has received regulatory approval from the Drugs Controller General of India (DCGI) to commence two Phase...

Lupin Limited Secures U.S. FDA Nod for Glycerol Phenylbutyrate Oral Liquid in Urea Cycle Disorders

Lupin has announced that it has received approval from the United States Food and Drug Administration (U.S. FDA) for its Abbreviated New Drug Application...

New Meta-Analysis Ranks CAPLYTA®️ Lumateperone First in Efficacy and Metabolic Safety for Adjunctive MDD Treatment

Intra-Cellular Therapies, Inc. announced the presentation of a new network meta-analysis (NMA) demonstrating that CAPLYTA® (lumateperone) showed the greatest improvement across four key efficacy outcomes among...

GloGen Clinical Research Reports USFDA EIR with ‘Closed’ Status Following February Inspection

GloGen Clinical Research Pvt. Ltd. has received the Establishment Inspection Report (EIR) from USFDA, with the determination of “Closed”, auditorium conducted on 09th -13th...

Intervein Clears USFDA Inspection, Strengthens Global Standards in IVRT & IVPT

Intervein Research Labs Pvt. Ltd. has successfully completed a recent inspection by the U.S. Food and Drug Administration, marking a key milestone in its regulatory...