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The World Health Organization (WHO) on Friday (30 April) listed the Moderna Covid-19 vaccine for emergency use, making it the fifth vaccine to receive emergency validation from the WHO.
In December 2020, the US Food and Drug Administration issued an emergency use authorisation for the Moderna vaccine, while the European Medicines Agency granted it a marketing authorisation valid throughout the European Union in January this year.
Before being validated for the WHO Emergency Use Listing (EUL), the Moderna vaccine was already reviewed in January by WHO's Strategic Advisory Group of Experts on Immunisation (SAGE), which makes recommendations for vaccines' use in populations.
WHO's EUL procedure assesses the late phase II and phase III clinical trial data as well as substantial additional data on safety, efficacy, quality and a risk management plan of Covid-19 vaccines.
In addition to the Moderna vaccine, the WHO has previously listed the Pfizer/BioNTech, Astrazeneca-SK Bio, Serum Institute of India and Janssen vaccines for emergency use.
(This story has been published from a wire agency feed without modifications to the text. Only the headline has been changed.)
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