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WHO panel recommends Emergency Use Listing status for Bharat Biotech’s Covaxin

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WHO panel recommends Emergency Use Listing status for Bharat Biotech’s Covaxin

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WHO panel recommends Emergency Use Listing status for
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WHO panel recommends Emergency Use Listing status for Covaxin.

Covaxin, India’s indigeneously developed coronavirus vaccine by Bharat Biotech, has been recommended for emergency use listing by the World Health Organisation (WHO). The Technical Advisory Group of WHO on Wednesday recommended Covaxin for emergency use status, according to PTI.

The Technical Advisory Group (TAG), an independent advisory committee of the World Health Organisation (WHO), recommended Emergency Use Listing (EUL) status for Bharat Biotech COVID-19 vaccine Covaxin, sources in the know of the development said.

The WHO is in the process of evaluating Covaxin’s clinical trial data for use of  EUL.

The TAG on October 26 had sought “additional clarifications” from the company for Covaxin to conduct a final “risk-benefit assessment” for Emergency Use Listing of the vaccine.

“The Technical Advisory Group of WHO has recommended Emergency Use Listing status for Covaxin,” a source told PTI.

The TAG-EUL is an independent advisory group that provides recommendations to WHO on whether a COVID-19 vaccine can be listed for emergency use under the EUL procedure.

Earlier today, Bharat Biotech said the Central Drugs Standard Control Organisation (CDSCO) has approved the extension of shelf life of its COVID-19 vaccine Covaxin up to 12 months from the date of manufacture.

Bharat Biotech was initially given permission for the sale and distribution of Covaxin with a shelf life of six months, which was later extended to nine months, a company spokesperson told PTI.

“The CDSCO has approved the extension of shelf life of Covaxin up to 12 months, from the date of manufacture. This approval of shelf life extension is based on the availability of additional stability data, which was submitted to CDSCO,” Bharat Biotech said in a tweet.

The shelf life extension has been communicated to “our stakeholders,” it added.

The approval for the extension of shelf life of the vaccine comes ahead of crucial World Health Organisation (WHO) meeting for a final risk-benefit assessment for the emergency use listing (EUL) for the vaccine.

The WHO’s Technical Advisory Group for EUL last week had sought additional clarifications from Bharat Biotech for Covaxin.

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