Washington (US), May 10 (ANI: The US Food and Drug Administration (FDA) has authorized the use of antigen test for the first time to detect and treat COVID-19 infection.
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.
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
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
Bengaluru (Karnataka) [India], Nov 5 (ANI): Biopharmaceuticals major Biocon Ltd said on Tuesday it has received an establishment inspection report from the US Food and Drug Administration (FDA) for its biologics drug product facility here, reaffirming its global scale manufacturing capabilit
Washington DC, [USA] July 31 (ANI): The US Food and Drug Administration (FDA) has warned against the use of devices that promise 'vaginal rejuvenation', stating that it can cause serious effects.
Washington D.C. [USA], May 31 (ANI): United States President Donald Trump on Wednesday signed a major drug bill called "Right to Try" for terminally ill patients, allowing them to go for experimental medical treatments, which is not yet approved by the US Food and Drug Administration (FDA