Mumbai (Maharashtra) [India], November 20 (ANI/PRNewswire): Datar Cancer Genetics, a leading cancer research company today announced that the US Food and Drug Administration (FDA) has granted 'Breakthrough Designation' for its blood test to detect early-stage Breast Cancer.
New Delhi [India], November 6 (ANI): Bharat Biotech's US partner Ocugen has announced that it had asked the US Food and Drug Administration (FDA) for Emergency Use Authorisation (EUA) of Covaxin for children below 18.
Washington [US], November 4 (ANI): Following formal recommendation of the Pfizer COVID-19 vaccine for children 5-11 by the US Food and Drug Administration (FDA), and the Centers for Disease Control (CDC), US President Joe Biden on Thursday (local time) urged parents and guardians to get thei
Washington [US], November 3 (ANI): Following rigorous review and authorization process by the US Food and Drug Administration (FDA), the Centers for Disease Control (CDC) on Tuesday (local time) has formally recommended the Pfizer COVID-19 vaccine for children 5-11.
Washington [US], October 21 (ANI): The US Food and Drug Administration (FDA) approved the use of third doses of the Moderna and Johnson and Johnson (Janssen) vaccines against the novel COVID-19 for eligible individuals.
Washington [US], September 23 (ANI): US Food and Drug Administration (FDA) on Wednesday (local time) authorized booster shots of the Pfizer COVID-19 vaccine for those aged 65 and older and adults at high risk.
Washington [US], August 13 (ANI/Sputnik): The US Food and Drug Administration (FDA) has authorized the emergency use of the third dose of both Moderna and Pfizer vaccines against COVID-19 for immunocompromised people.
Washington [US], July 13 (ANI): The US Food and Drug Administration (FDA) on Monday (local time) warned coronavirus vaccine maker Johnson & Johnson of possible rare neurological complications caused due to its dose.
Washington [US], June 11 (ANI): A third member of the US Food and Drug Administration (FDA) expert advisory panel resigned from the body after it approved a controversial Alzheimer's drug named Aduhelm recently.
Pennsylvania [US], June 11 (ANI): Bharat Biotech's US partner Ocugen Inc said that the company will no longer pursue an Emergency Use Authorization (EUA) for COVAXIN and the US Food and Drug Administration (FDA) has recommended that the company go for the Biologics Licence Application (BL
Washington [US], May 31 (ANI): Amid mounting concerns regarding a renewed probe of the origins of COVID-19 in China, former US Food and Drug Administration (FDA) Commissioner Scott Gottlieb said that accidental lab leaks 'happen all the time' and there have been six last known outbreaks of S