Merck receives positive EU CHMP opinion for expanded use of Winrevair in adults with Pulmonary Arterial Hypertension Written By Ruchika Sharma14 Dec 2025 12:45 PM ISTRahway: Merck, known as MSD outside of the United States and Canada, has announced that the European Medicines Agency’s Committee for Medicinal...
Sanofi gets approval for 2 rare hematologic diseases medicines in China Written By Ruchika Sharma14 Dec 2025 11:30 AM ISTThese two approvals expand Sanofi's rare hematology portfolio in China.
CDSCO Launches Online Risk Classification Module for Non-IVD Medical Devices Written By Susmita Roy14 Dec 2025 12:48 AM ISTNew Delhi: In a significant step toward streamlining India's medical device regulatory ecosystem, the Central Drugs Standard Control Organisation...
Novo Nordisk Gets CDSCO Panel Nod to Update Wegovy Label With New Safety, Pharmacodynamics Data Written By Susmita Roy14 Dec 2025 12:43 AM ISTNew Delhi: The Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO) has recommended granting approval to Novo...
GSK Nucala receives positive EMA Committee opinion for COPD Written By Ruchika Sharma13 Dec 2025 3:32 PM ISTLondon: GSK has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended the...
Aurobindo Pharma arm API facility receives 3 observations from USFDA Written By Ruchika Sharma13 Dec 2025 12:58 PM ISTHyderabad: Aurobindo Pharma has announced that the United States Food and Drug Administration (USFDA) concluded the inspection with three...
Dr Reddy's Labs gets 5 USFDA observations for Srikakulam facility Written By Ruchika Sharma13 Dec 2025 12:17 PM ISTHyderabad: Dr Reddy's Labs has announced that the United States Food & Drug Administration (USFDA) has completed a GMP and a...
GSK Blujepa gets USFDA approval as oral option for uncomplicated urogenital gonorrhoea Written By Ruchika Sharma13 Dec 2025 11:30 AM ISTLondon: GSK has announced that the US Food and Drug Administration (FDA) has approved a supplemental New Drug Application for gepotidacin as an...
Granules Life Sciences facility receives EIR from USFDA Written By Ruchika Sharma13 Dec 2025 10:30 AM ISTHyderabad: Granules India has announced that Granules Life Sciences Private Limited, a wholly owned subsidiary of the company situated in...
Govt Sanctions Rs 181.59 Cr for Pharma Upgrades Under RPTUS, Parliament Informed Written By Parthika Patel12 Dec 2025 9:31 PM ISTNew Delhi: A total of 192 applications has been approved so far, with a total sanctioned amount of Rs 181.59 crore under the Government's Revamped...
PCI Allows One-Year Provisional Registration for D.Pharm Students Amid Exit Exam Delay Written By Parthika Patel12 Dec 2025 9:07 PM ISTNew Delhi: In a major relief for Diploma in Pharmacy (D.Pharm) students, the Pharmacy Council of India (PCI) has decided to allow one-year provisional...
Himachal cracks down on pharma units, action taken against four facilities Written By Parthika Patel12 Dec 2025 8:57 PM ISTShimla: In a major statewide crackdown under the anti-drug campaign launched on November 15, Himachal Pradesh authorities on Wednesday inspected 20...
