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WHO approves AstraZeneca COVID-19 vaccine for emergency use

by Health Business
February 16, 2021
in News
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WHO approves AstraZeneca COVID-19 vaccine for emergency use
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The World Health Organization (WHO) on Monday gave the green light to two versions of the AstraZeneca/Oxford COVID-19 vaccine for emergency use, allowing them to be rolled out globally via COVAX.

The two versions are produced by AstraZeneca-SKBio in South Korea and the Serum Institute of India, WHO said in a news release, noting that the vaccine shows 63.09 percent efficacy and “is suitable for low- and middle-income countries due to easy storage requirements.”

The vaccine can now be used via COVAX, a WHO-led international initiative for equitable access to COVID-19 vaccines, said Dr. Mariangela Simao, WHO assistant-director general for Access to Medicines and Health Products.

“Countries with no access to vaccines to date will finally be able to start vaccinating their health workers and populations at risk,” said Simao.

“But we must keep up the pressure to meet the needs of priority populations everywhere and facilitate global access,” she said. And to this end, she sorted out two priorities: a scale-up of manufacturing capacity, and developers’ early submission of their vaccines for WHO review. The AstraZeneca product is the second Covid-19 jab to have received WHO authorization, after Pfizer/BioNTech vaccine in late December.(Xinhua)

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Health Business

Health Business contains need-to-know features, news and case studies that explain the administrative and commercial issues affecting healthcare and hospital management. Health Business supports several high profile exhibitions - coverage of which is always timed for maximum impact. Regular topics include ICT, Finance/Funding, Facilities Management, Security, Health & Safety. Contributors range from government ministers through to top-level health administrators and association chairs.

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