(Reuters) – AstraZeneca Plc may skip asking the U.S. Food and Drug Administration for emergency-use authorization for its COVID-19 vaccine, and instead pursue the more time-intensive application for a full-fledged license to sell the shot, the Wall Street Journal reported on Friday. Such a step would further delay any rollout of the British drugmaker's shots in the United States, according to the report https://on.wsj.com/3eWvrry, which cited people familiar with the matter. (Reporting by Kanish

https://wsau.com/2021/05/07/astrazeneca-weighs-seeking-full-u-s-approval-for-covid-19-shot-wsj/

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