The US Food and Drug Administration's advisory panel, comprising external experts, has given an emergency use approval to Moderna COVID-19 vaccine, making it the second drug after Pfizer to receive such an authorisation in less than a week.
from World News Headlines, Latest International News, World Breaking News - Times of India https://ift.tt/34m3Zim
from World News Headlines, Latest International News, World Breaking News - Times of India https://ift.tt/34m3Zim
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