Geneva (Switzerland):The World Health Organisation (WHO) on Friday approved the Chinese Sinopharm COVID-19 vaccine for emergency use, paving the way for it to be rolled out globally.
The Sinopharm vaccine is produced by Beijing Bio-Institute of Biological Products Co Ltd, a subsidiary of China National Biotec Group (CNBG).
"The addition of this vaccine has the potential to rapidly accelerate COVID-19 vaccine access for countries seeking to protect health workers and populations at risk," said Dr Mariangela Simao, WHO Assistant-Director General for Access to Health Products, in a statement.
"We urge the manufacturer to participate in the COVAX Facility and contribute to the goal of more equitable vaccine distribution," she added. This comes amid growing criticism of the Sinopharm vaccine. The WHO's Emergency Unit Listing (EUL) allows countries to expedite their own regulatory approval to import and administer COVID-19 vaccines.
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It assesses the quality, safety and efficacy of COVID-19 vaccines, as well as risk management plans and programmatic suitability, such as cold chain requirements.
The global health body recommended the Chinese vaccine for adults 18 years and older, in a two-dose schedule with a spacing of three to four weeks. Vaccine efficacy for symptomatic and hospitalised disease was estimated to be 79 per cent, all age groups combined.