FDA issues emergency use authorization for Johnson & Johnson vaccine
Good Morning America – February 28, 2021 Medical experts on Friday unanimously recommended that drug regulators clear Johnson & Johnson’s COVID-19 vaccine for Emergency Use Authorization (EUA); Saturday, EUA was granted. The vaccine was developed in a collaboration between Johnson & Johnson and BIDMC, led by Dan Barouch, MD, PhD (Center for Virology and Vaccine Research, BIDMC).
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CBS Boston – Advisers endorse single-shot COVID-19 vaccine from Johnson & Johnson MIT Technology Review – The one-shot vaccine from Johnson & Johnson now has FDA support in the US