WHO seeks additional information on Covaxin from Bharat Biotech
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United Nations/Geneva: The World Health Organisation on Monday said it was expecting additional information from India's Bharat Biotech regarding its COVID-19 jab Covaxin, asserting that it "cannot cut corners" before recommending a vaccine for emergency use.
The global health agency also emphasized that it must evaluate a vaccine thoroughly to make sure it is "safe and effective".
Hyderabad-based Bharat Biotech, which has developed Covaxin, had submitted EOI (Expression of Interest) to the WHO on April 19 for the vaccine's Emergency Use Listing (EUL).
In a series of tweets, WHO said, "we are aware that many people are waiting for WHO's recommendation for Covaxin to be included in the #COVID-19 Emergency Use Listing, but we cannot cut corners - before recommending a product for emergency use, we must evaluate it thoroughly to make sure it is safe and effective."
It also said that Bharat Biotech has been submitting data to WHO on a rolling basis and WHO experts have reviewed these data.
"The technical advisory group will meet on Oct 26th to consider EUL for #Covaxin. @WHO has been working closely with @BharatBiotech to complete the dossier. Our goal is to have a broad portfolio of vaccines approved for emergency use & to expand access to populations everywhere," she said.
Bharat Biotech last month said it has submitted all data pertaining to Covaxin to the WHO for EUL and is awaiting feedback from the global health watchdog.
"#COVAXIN clinical trial data was fully compiled & available in June 2021. All data was submitted for EUL application to WHO in early July. We have responded to any clarifications sought by #WHO and are awaiting further feedback," it said in a tweet.
"We are diligently working with the WHO to obtain EUL at the earliest," the company added.
Covaxin is one of the two anti-COVID vaccines used by India in its vaccination drive across the country.
Earlier this month, WHO had said in a tweet that Bharat Biotech "has been submitting data to WHO on a rolling basis & submitted additional info,..on 27 September. WHO experts are currently reviewing this info & if it addresses all questions raised, WHO assessment will be finalized next week."
Rolling data allows the WHO to start its review right away, as information continues to come in, to accelerate the overall review process.
According to WHO, submissions for pre-qualification or listing under the EUL procedure are confidential and if a product submitted for assessment is found to meet the criteria for listing, WHO will publish the results widely.
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