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, || Vaccines cleared amidst questions? ||
The much-awaited emergency licence for a Covid-19 vaccine in India is only a matter of time, now that the subject expert committee of the Drug Controller General of India (DCGI) has recommended it for the Oxford-AstraZeneca candidate Covishield and for Bharat Biotechs Covaxin.
The health ministry, in a statement said, the subject expert committee of the drugs regulator, Central Drugs Standard Control Organisation (CDSCO), has made the following recommendations for the consideration and final decision of the Drugs Controller General of India (DGCI) grant of permission for restricted emergency use of vaccine, subject to multiple regulatory conditionalities, to Serum Institute of India; grant of permission for restricted use in emergency situation in public interest as an abundant precaution, in clinical trial mode, specially in the context of infection by mutant strains, to Bharat Biotech; and grant of permission to conduct Phase 3 clinical trials to Cadila Healthcare.
However, for the average Indian aged less than 50 years and without any comorbidities, the wait for a jab is likely to extend till 2022.
The initial vaccine supply, even with two suppliers, is likely to be very slow and there is currently no clarity on when a shot can be bought at a pharmacy by a person who is not on the priority list.
The Government, according to sources, is keen that all the vaccines that become available now should be used to inoculate the four priority groups of vulnerable people health workers, other Covid warriors like police, those aged over 50 years, and people of all ages with comorbidities.
What next as govt expert panel gives conditional nod for Covid vaccines Covaxin and Covishield
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You can enroll as a voter for MLC elections now if you have not enrolled earlier. https://ceotserms1.telangana.gov.in/MLC/Form18.aspx , || Vaccines cleared amidst questions? || The much-awaited emergency licence for a Covid-19 vaccine in India is only a matter of time, now that the subject expert committee of the Drug Controller General of India (DCGI) has recommended it for the Oxford-AstraZeneca candidate Covishield and for Bharat Biotechs Covaxin. The health ministry, in a statement said, the subject expert committee of the drugs regulator, Central Drugs Standard Control Organisation (CDSCO), has made the following recommendations for the consideration and final decision of the Drugs Controller General of India (DGCI) grant of permission for restricted emergency use of vaccine, subject to multiple regulatory conditionalities, to Serum Institute of India; grant of permission for restricted use in emergency situation in public interest as an abundant precaution, in clinical trial mode, specially in the context of infection by mutant strains, to Bharat Biotech; and grant of permission to conduct Phase 3 clinical trials to Cadila Healthcare. However, for the average Indian aged less than 50 years and without any comorbidities, the wait for a jab is likely to extend till 2022. The initial vaccine supply, even with two suppliers, is likely to be very slow and there is currently no clarity on when a shot can be bought at a pharmacy by a person who is not on the priority list. The Government, according to sources, is keen that all the vaccines that become available now should be used to inoculate the four priority groups of vulnerable people health workers, other Covid warriors like police, those aged over 50 years, and people of all ages with comorbidities. https://theprint.in/india/governance/what-next-as-govt-expert-panel-gives-conditional-nod-for-covid-vaccines-covaxin-and-covishield/577895/