New Delhi [India], May 4 (ANI): Union Health Minister Dr Harsh Vardhan on Monday discussed among other things the progress over Remdesivir -- antibody-drug recently approved by the US-FDA for emergency use to treat COVID-19 patients -- with the heads of Council of Scientific and Industria
California [USA], May 2 (ANI): US-based biopharmaceutical major Gilead Sciences said that the US Food and Drug Administration (FDA) has granted emergency use authorisation (EUA) for investigational anti-viral remdesivir to treat COVID-19.
Washington D.C. [US], May 2 (Sputnik/ANI): The US Food and Drug Administration has authorized an emergency use of Remdesivir drug in coronavirus treatment, FDA head Stephen Hahn announced on Friday.
Basel [Switzerland], April 22 (ANI): Swiss multinational pharmaceutical company Novartis has reached an agreement with the US Food and Drug Administration (FDA) to proceed with a phase three clinical trial with about 440 patients to evaluate the use of hydroxychloroquine for the treatment of
New Delhi [India], April 20 (ANI): Indian Council of Medical Research (ICMR) on Monday said that RTPCR kits are US FDA approved and have good standards and these should be stored under 20-degree temperature for better result.
Mumbai (Maharashtra) [India] April 14 (ANI/NewsVoir): MSB Docs - a smart document solution officially entered the Indian market in 2019 and in such a short time span, it has started serving top brands including Apollo Hospitals, Practo, Bits Pilani, Alkem Laboratories, CORE Diagnostics, and
Washington DC [USA], April 11 (ANI): The US Food and Drug Administration (FDA) on Saturday authorised emergency use of a blood purification device to treat COVID-19 patients who are above 18 years of age. The treatment has been only authorised for patients admitted in the Intensive-Care Unit
Mumbai (Maharashtra) [India], Apr 3 (ANI): Pharma major Lupin Ltd said on Friday it has got an establishment inspection report (EIR) from the US Food and Drug Administration for its Aurangabad facility.
Bengaluru (Karnataka) [India], Mar 30 (ANI): Strides Pharma Science Ltd said on Monday it has received the establishment inspection report (EIR) conducted by the US Food and Drug Administration last month at the company's flagship facility.
Mumbai (Maharashtra) [India], Mar 27 (ANI/ PRNewswire): Cipla Limited (BSE: 500087) (NSE: CIPLA EQ) and hereafter referred to as "Cipla" today announced that it has received final approval for its Abbreviated New Drug Application (ANDA) for Esomeprazole for Oral Suspension 10mg, 20mg and 40m
Washington D.C. [US], Mar 20 (ANI): As the number of coronavirus cases in the US continued to rise, President Donald Trump on Thursday said that hydroxychloroquine, an anti-malarial drug, can potentially be effective for treating coronavirus.
New Delhi [India], Mar 18 (ANI): Amid coronavirus fears, international private diagnostic centres are coming forward to conduct the COVID-19 tests in India.