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'WHO's emergency use authorization to Covaxin expected soon'

By ANI | Updated: September 24, 2021 21:10 IST

The Union Health Ministry on Friday hinted that World Health Organization's emergency use authorization to Covaxin is expected soon.

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The Union Health Ministry on Friday hinted that World Health Organization's emergency use authorization to Covaxin is expected soon.

However, the World Health Organisation's (WHO) approval for the emergency use authorisation (EUA) to Covid-19 vaccine, Covaxin, is likely to be delayed as per international public health agency. In this regard, the Strategic Advisory Group of Expert on Immunization (SAGE) will be meeting on October 5 to grant EUA to Covaxin.

"There is a procedure of submitting the documents for approval. WHO's emergency use authorization to Covaxin is expected soon," said Dr Bharati Pravin Pawar who is currently the Union Minister of State in the Health Ministry.

According to Bharat Biotech, Phase-3 clinical trials of Covaxin demonstrated an efficacy rate of 77.8 per cent.

All the relevant trial data has been submitted to WHO for Emergency Use Listing (EUL) and all clarifications by the UN health agency have been responded to Bharat Biotech.

"We have responded to clarifications sought by WHO and are awaiting further feedback. As a responsible manufacturer with several prequalified vaccines, we do not find it appropriate to speculate or comment on the approval process and its timelines," the Hyderabad based company said in a statement.

Earlier speaking to ANI, Chairperson of National Expert Group on Vaccine Administration and Member of Health for NITI Aayog, Dr VK Paul said that the WHO's approval for Bharat Biotech's COVID-19 vaccine, Covaxin is likely to come before the end of this month.

The WHO has approved COVID-19 vaccines by Pfizer-BioNTech, AstraZeneca, Johnson and Johnson, Moderna and Sinopharm till date.

As of date, India is using three vaccines against COVID-19 in its immunization drive. These include two made-in-India vaccines - Serum Institute of India's Covishield and Bharat Biotech's Covaxin. The Russian Sputnik V is the third vaccine that got approval from the Drug Controller General of India (DCGI) for Emergency Use Authorisation.

In Phase I of the vaccination drive, started on January 16, the National Expert Group on Vaccine Administration for Covid-19 (NEGVAC) prioritised Health Care Workers and Front Line Workers (both government and private sector).

Phase II of the vaccination drive started from March 1 2021, focused on protecting the most vulnerable age groups. These prioritised age-groups included persons above 60 years of age and persons above 45 years with associated specified co-morbidities. This was further relaxed to all people above 45 years of age on April 1, 2021.

In Phase III, 'Liberalised Pricing and Accelerated National COVID-19 Vaccination Strategy' was adopted on May 1, 2021. Under this strategy, everyone above 18 years of age are eligible for COVID-19 vaccination.

( With inputs from ANI )

Disclaimer: This post has been auto-published from an agency feed without any modifications to the text and has not been reviewed by an editor

Tags: indiaHyderabadUnion Health MinistryWorld Health OrganizationNagarWhoWorld healthU of u healthFinance and healthHyder
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