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India Coronavirus Dispatch: How emergency vaccine authorisation works

Queues at Ahmedabad's crematoriums get longer, doubts about AstraZeneca vaccine and bringing diagnostics closer to communities-news relevant to India's fight against Covid-19

Coronavirus, vaccine, covid, drugs, clinical trials
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With the end of India’s fight against Covid-19 not yet in sight, the resilience of the country’s health systems is faced with a serious test,

Bharath Manjesh New Delhi
What is the emergency use authorisation drugmakers are seeking for the Covid-19 vaccine?

Vaccines, like medicines, require the approval of a regulatory authority before these can be administered. In India, the top regulatory authority is the Central Drugs Standard Control Organisation, or CDSCO.

In the case of vaccines, and also medicines, the approval is granted after an assessment of its safety and effectiveness, based on data generated from trials on animals and human beings. In fact, approval from the regulator is required at every stage of these trials. This is a long process, designed to ensure that medicine or vaccine is absolutely