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IndiaPosted at: Jan 20 2022 12:22AM


Central drug authority recommends regular marketing approval of Covishield, Covaxin

New Delhi, Jan 19 (UNI) The Subject Expert Committee (SEC) under the Central Drug Regulatory Authority recommended upgrading the status of Covid-19 vaccines Covishield and Covaxin from restricted emergency use to regular marketing authorisation with certain conditions, the Central Drugs Standard and Control Organisation (CDSCO) said on Wednesday.
The central body also said the recommendations will be evaluated by the Drug Controller General of India (DCGI) before the final decision.
"SEC of CDSCO has recommended for upgrade of Covishield and Covaxin status from restricted use in emergency situations to grant new drug permission with conditions in adult population," the CDSCO posted on Twitter.
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Tags: #Central drug authority recommends regular marketing approval of Covishield# Covaxin
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