CDSCO expert panel to meet today to review data on Serum Institute, Bharat Biotech COVID-19 vaccines
Photo Credit: AFP

An expert panel in the Central Drugs Standard Control Organisation (CDSCO) will meet again on Friday to take a decision on the emergency-use authorisation (EUA) application of Serum Institute of India’s (SII) Oxford-AstraZeneca and Bharat Biotech’s vaccine candidates against Coronavirus.

Today's meeting comes a day before a dry run for vaccinations in all states. At an event on Thursday, Drugs Controller General Dr VG Somani said, "Probably we will have a happy New Year with something in hand. That is what I can hint at".

The Subject Expert Committee had met on Wednesday to consider the Emergency Use Authorisation (EUA) request of Pfizer, SII and Bharat Biotech Private Ltd. The SII, Bharat Biotech and Pfizer have applied to the DCGI seeking emergency use authorisation for their COVID-19 vaccine candidates and are awaiting approval.

The Subject Expert Committee (SEC) on COVID-19 deliberated and analysed the additional data and information submitted by Serum Institute of India (SII) and Bharat Biotech. "The Subject Expert Committee (SEC) in the CDSCO met today in the afternoon to consider the emergency use authorisation (EUA) request of Pfizer, Serum Institute of India (SII) and Bharat Biotech Pvt. Ltd," the Health Ministry had said in a statement.

"Further time was requested on behalf of Pfizer. The additional data and information presented by SII and Bharat Biotech Pvt. Ltd was perused and analysed by the SEC. The analysis of the additional data and information is going on. The SEC will convene again on January 1, 2021," it said.

The Pune-based Serum Institute of India (SII), the world's largest vaccine manufacturer, has entered into a tie-up AstraZeneca to manufacture 'Covishield'. While considering SII's application, the SEC on December 9 had recommended that the firm should submit updated safety data of phase 2 and 3 clinical trials in the country, immunogenicity data from the clinical trial in the UK and India, along with the outcome of the assessment of the UK MHRA for grant of EUA.

As for Hyderabad-based Bharat Biotech, after detailed deliberation, the committee had recommended that the firm should present the safety and efficacy data from the ongoing phase 3 clinical trial in the country for further consideration.

SII had applied to the Drugs Controller General of India (DCGI) for emergency use authorisation for Covishield on December 6 while the Hyderabad-based Bharat Biotech had sought a similar nod for its indigenously developed Covaxin on December 7. Pfizer had applied for a similiar approval for its vaccine on December 4.

(To receive our E-paper on whatsapp daily, please click here. We permit sharing of the paper's PDF on WhatsApp and other social media platforms.)

Free Press Journal

www.freepressjournal.in