Johnson & Johnson has secured an emergency use authorization (EUA) for its Janssen COVID-19 vaccine from the Food and Drug Administration (FDA), Secretary Carlito Galvez Jr., the country’s vaccine manager, said Monday. Video by RTVM | INQUIRER.net
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BREAKING NEWS: The Janssen #COVID19 vaccine has been authorised for use in the UK by Medicines & Healthcare products Regulatory Agency ✅ This follows clinical trials and analysis of the vaccine’s safety, quality and effectiveness. Deliveries are expected later this year. Read more: https://www.gov.uk/government/news/janssen-coronavirus-covid-19-vaccine-authorised-by-uk-medicines-regulator | Department of Health and Social Care - DHSC
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Johnson & Johnson announced that the CDC Advisory Committee recommends our single-dose COVID-19 vaccine for individuals age 18 and older, under the Emergency Use Authorization issued by the U.S. FDA. Read more: https://bit.ly/3r8ovfO The Janssen COVID-19 Vaccine has not been approved or licensed by FDA: https://bit.ly/2NKFjLs | Johnson & Johnson
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