California [US], September 30 (ANI): A team of researchers found that the drug tofacitinib, also called Xeljanz and approved by the FDA to treat rheumatoid arthritis and ulcerative colitis, can repair permeability defects in the intestine.
New Delhi [India] September 25 (ANI/NewsVoir): AliveCor, the global leader in US FDA-cleared personal electrocardiogram (ECG) technology, today announced its entry in the Indian market with the revolutionary launch of the most clinically-validated personal ECG device, KardiaMobile 6L.
Washington [US], September 24 (ANI/Sputnik): US President Donald Trump ON Wednesday (local time) said that his administration may or may not approve a proposal from the Food and Drug Administration (FDA) that would tighten guidelines for approving a novel coronavirus disease (COVID-19) vacci
Washington D.C. [US], August 24 (ANI): The US Food and Drug Administration (FDA) has authorised the use of convalescent plasma for the treatment of COVID-19 patients.
Washington DC [US], Aug 23 (ANI): US President Donald Trump will hold a press conference on Sunday concerning a "major therapeutic breakthrough" on coronavirus, the White House said.
Washington [US], Aug 23 (ANI): US President Donald Trump on Saturday (local time) slammed the Food and Drug Administration (FDA) for trying to slow down the human trials of coronavirus vaccines.
Washington [US], August 16 (ANI/Sputnik): The United States' Food and Drug Administration (FDA) has approved a new COVID-19 testing method based on analysing saliva samples.
Bengaluru (Karnataka) [India], Aug 2 (ANI): Bengaluru based Centre for Advanced Research and Development (CARD), the research wing of organisation De scalene has come up with a device called "SHYCOCAN" (Scalene Hypercharge Corona Canon) which neutralizes the coronavirus.
Washington D.C. [USA], July 19 (ANI): The US Food and Drug Administration (FDA) on Saturday (local time) issued an emergency use authorisation (EUA) to Quest Diagnostics that allows pool samples from up to four individuals to test for COVID-19.
Panaji (Goa) [India], July 19 (ANI): Goa Food and Drugs Administration has urged people, chemists, and druggists that rapid diagnostic kits approved by the Indian Council of Medical Research and DCGI must be used.
Mumbai (Maharashtra) [India], July 7 (ANI): Indian pharmaceutical companies have built a strong abbreviated new drug application (ANDA) pipeline since FY12 through scaling-up of investments in R&D but this will increase the inspection intensity, India Ratings and Research (Ind-Ra) said o
Bengaluru (Karnataka) [India], July 7 (ANI): Global pharmaceutical major Mylan has got approval for its remdesivir from the Drug Controller General of India (DCGI) and will launch a generic version of Gilead Sciences' COVID-19 anti-viral in the country at Rs 4,800 for 100 mg/vial.