US regulator FDA clears Johnson & Johnson's single-dose COVID vaccine for emergency use


U.S. regulators on Saturday authorized a third COVID-19 vaccine, a single-dose shot by Johnson & Johnson that could help speed vaccinations. The move by the Food and Drug Administration came after an expert panel debated the evidence to allow widespread use of J&J’s vaccine. J&J has said it can supply enough to vaccinate 20 million people by the end of March.





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