US FDA approves five-minute ‘Rapid’ coronavirus COVID-19 test
The company has also been given the US Food and Drug Administration's approval as 'emergency use authorisation' for the test.
Mar 28, 2020, 10:29 AM IST
In a first, US regulators approve pill that digitally tracks patients' medication intake
Poor compliance with drug regimens is a common problem in many disease areas, especially when patients suffer from chronic conditions.
Nov 14, 2017, 18:52 PM IST
US FDA accepts application for psoriasis drug: Sun Pharma
Drug major Sun Pharmaceutical Industries on Wednesday said the US health regulator has accepted biologics licence application (BLA) for tildrakizumab for the treatment of psoriasis.
May 24, 2017, 11:49 AM IST
Coming very soon! Luke prosthetic arm that will change lives of amputees (Watch video)
Previously known as the Deka Arm, the Luke arm - developed by Segway creator Dean Kamen and DARPA (the Defense Advanced Research Projects Agency) - integrates the latest technology in electronics, motors, batteries, and materials.
Jul 12, 2016, 10:28 AM IST
DRL says taking corrective actions after FDA warning letter
DRL shares on Monday stumbled by 3.44 percent over previous close to Rs 3,504.60 on BSE.
Nov 09, 2015, 21:12 PM IST
Unichem gets USFDA nod for hypertension treatment tablets
Pharmaceutical firm Unichem Laboratories has received US FDA approval for the Losartan Potassium tablets used in treatment of hypertension.
Oct 16, 2015, 12:55 PM IST
IPCA Labs aims to make plants US FDA-compliant by December
IPCA Laboratories Ltd is aiming to make all of its plants facing import alerts from the United States compliant with U.S. Food and Drug Administration (FDA) rules by December, an executive said on Wednesday.
Mar 25, 2015, 13:51 PM IST
IPCA slumps as FDA bans imports from 2 more plants
Shares in generic drugmaker IPCA Laboratories slumped as much 12.7 percent, heading towards their biggest daily fall since July 2014, after the U.S. Food and Drug Administration (FDA) issued an import alert against two of its plants.
Mar 25, 2015, 13:18 PM IST
US FDA did not find issues with Wockhardt's Chikalthana plant
"The recent inspection at the Aurangabad L1-Chikalthana site was a follow-up inspection by the US FDA as an outcome of completion of good manufacturing practise (GMP) remediation submitted by Wockhardt in October 2014.
Mar 18, 2015, 19:03 PM IST
FDA raises concern over drug production process at Cadila
The FDA inspected the Moraiya plant, based in Gujarat, in the second week of July.
Jul 31, 2014, 13:11 PM IST
