The United States Food and Drug Administration (US FDA) has flagged serious concerns at Dabur India's manufacturing facility in Silvassa, Dadra and Nagar Haveli, following an inspection conducted in...
Wockhardt Limited announced that the U.S. Food and Drug Administration (FDA) has approved ZAYNICH™ (cefepimeand zidebactam), a novel intravenous antibiotic...
Fatal Incidents Trigger Nationwide Cough Syrup Inspections by CDSCO
PharmaGenDRx News Bureau,8th October, 2025
06:00 PM IST
Following the recent reports of fatalities linked with the cough...
RAJASTHAN DOCTOR COLLAPSED AFTER CONSUMING COUGH SYRUP LINKED WITH CHILDREN'S DEATH
PharmaGenDRx, 4th October, 2025
6 PM IST
On September 24, 2025, Tuesday at Bayana Community Health...
TRADE TENSION RISES: TRUMP ANNOUNCES 100% TARRIF ON IMPORTED MEDICINES
PharmaGenDRx News Bureau- 27th September,2025
12:00 PM IST
On Thursday, 25th of September, 2025, in a rally...
CCRAS Highlights Pediatric ADR Vigilance on World Patient Safety
PharmaGenDRx News Bureau- 22nd September,2025
2:00 PM IST
To mark World Patient Safety Day 2025, the central Council...
Special Campaign 5.0 Preparation Begins Across Department of Pharmaceuticals
PharmaGenDRx News Bureau-16th September,2025
3:00 PM IST
The Department of Pharmaceuticals (DoP) under the directory of the Ministry...
Global Collaboration to Drive India's MedTech Vision: Says Shri Amit Agrawal
PharmaGenDRx News Bureau- 24th August, 2025
2:00 PM IST
Addressing a regional meet on “Health Research...