After drugmakers applied for full FDA approval of their COVID-19 vaccines, the FDA took three months to deploy an "all hands on deck" strategy to work toward approval. A guest columnist says that must happen quickly to reassure those who are hesitant or skeptical of the vaccine.
NEW DELHI: India gave emergency approval to Johnson and Johnson's single-shot COVID-19 vaccine on Saturday (Aug 7) to ramp up its flailing immunisation campaign as fears grow of a new wave of infections.
Health minister Mansukh Mandaviya said the approval will boost the fight against the pandemic in India,
Johnson and Johnson s single-dose vaccine against Covid-19 has got the approval for emergency use in India on Saturday. With J&J single-dose vaccine, India has now a total of 5 Emergency Use Authorization vaccines (EUA) to strengthen the .
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