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India fast-tracks emergency use of foreign-made Covid-19 vaccines

In a significant move, the Union government on Tuesday allowed emergency use of foreign Covid-19 vaccines through a fast-track route, striking off the need for a prior local trial. In line with the recommendations of the National Expert Group on Vaccine Administration for COVID-19 (NEGVAC), vaccines which have been developed and are being manufactured in foreign countries, with approval from health regulators in the US, UK, European Union and Japan, would now be permitted for emergency use in India. Those in the World Health Organisation (WHO) emergency use list will also be allowed. Instead of prior local clinical trials, companies must do parallel clinical trials after vaccine enters the India market. Also, the first 100 beneficiaries of such foreign vaccines shall be assessed for seven days for safety outcomes before an expansion of the immunization programme, the health ministry said in a statement.

Russia s Sputnik V Get Expert Panel Clearance: Five Things to Know About India s Third Covid-19 Vaccine

Russia s Sputnik V Get Expert Panel Clearance: Five Things to Know About India s Third Covid-19 Vaccine News18 1 hour ago News18 © Provided by News18 Russia s Sputnik V Get Expert Panel Clearance: Five Things to Know About India s Third Covid-19 Vaccine Sputnik V vaccine developed by Russia against Covid-19 on Monday received approval from India for its emergency use with certain conditions. The decision was taken by Subject Expert Committee (SEC) of the Central Drugs Standard Control Organization (CDSCO) at a time when the country is witnessing record surge of infection cases. India currently manufactures two vaccines – Pune-based Serum Institute of India’s Covishield developed by Oxford-AstraZeneca and Hyderabad-based Bharat Biotech’s Covaxin. If approved by India’s regulator Drugs Controller General of India (DCGI), Sputnik V will become the third vaccine to be used in the country.

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