The WHO EUL process aims to determine the quality, safety and efficacy assurance of a manufactured product such as Covid Vaccine Covaxin from Bharat Biotech in this case.

WHO, EUL, Bharat Biotech, Covaxin, Dr Soumya Swaminathan, DCGI, EUAAccording to the WHO, applications to WHO for pre-qualification or inclusion under the EUA procedure are confidential. If a product submitted for evaluation is found to meet the inclusion criteria, the World Health Organization will publish the results widely.

To consider the Emergency Use List (EUL) for Bharat Biotech’s Covid vaccine Covaxin, the World Health Organization (WHO) technical advisory group will meet on October 26, WHO chief scientist Dr Soumya Swaminathan said recently.

The WHO EUL process aims to determine the quality, safety and efficacy assurance of a manufactured product such as Covid Vaccine Covaxin from Bharat Biotech in this case.

“Our goal is to have a wide range of vaccines approved for emergency use and expand access to populations everywhere,” said Dr Soumya Swaminathan.

Covaxin has not yet been approved by the Controller General of Drugs of India (DCGI) for emergency use authorization (EUA) in children and adolescents 2 to 18 years of age.

The World Health Organization had tweeted this month, “Bharat Biotech, has been providing data on a rolling basis and provided additional information at the request of the World Health Organization on September 27.”

Rolling data allows WHO to begin its review immediately, as information continues to come in, to speed up the overall review process.

According to the WHO, applications to WHO for pre-qualification or inclusion under the EUA procedure are confidential. If a product submitted for evaluation is found to meet the inclusion criteria, the World Health Organization will publish the results widely.

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