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Bharat Biotech seeks emergency use authorisation for Covaxin, days after Pfizer and SII

Bharat Biotech seeks emergency use authorisation for Covaxin, days after Pfizer and SII
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Bharat Biotech seeks emergency use authorisation for Covaxin, days after Pfizer and SII

Bharat Biotech seeks emergency use authorisation for Covaxin, days after Pfizer and SII

Final week, Prime Minister Narendra Modi had mentioned {that a} COVID-19 vaccine ‘could also be prepared in just a few weeks’ at an all-party assembly

Bharat Biotech seeks emergency use authorisation for Covaxin, days after Pfizer and SII

COVAXIN vaccine by Bharath Biotech.

New Delhi: After Pfizer and Serum Institute, Hyderabad-based pharmaceutical agency Bharat Biotech on Monday utilized to the central drug regulator Central Medicine Normal Management Organisation (CDSCO), searching for emergency use authorisation for its COVID-19 vaccine Covaxin, official sources mentioned.

Covaxin is being indigenously developed by Bharat Biotech in collaboration with the Indian Council of Medical Analysis (ICMR).

On 4 December, Prime Minister Narendra Modi at an all-party assembly had expressed hope {that a} COVID-19 vaccine could also be prepared in just a few weeks.

That very same night, the Indian arm of US pharmaceutical big Pfizer sought emergency use approval for its vaccine from the central drug regulator, after the agency secured such clearance within the UK and Bahrain.

The Serum Institute sought such nod for the Oxford COVID-19 vaccine, Covishield, on 6 December.

The functions of Bharat Biotech, Serum Institute of India and Pfizer shall be reviewed by the topic professional committee (SEC) on COVID-19 on the CDSCO within the coming days.

“Nonetheless, not one of the functions has to this point been forwarded to the committee and no date has been fastened as on when the SEC will meet for assessing and evaluating the functions,” the official supply mentioned.

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