As the country awaits the UK's approval to the AstraZeneca-Oxford vaccine before giving nod for Emergency Use Authorisation to its Indian counterpart developed by Pune-based Serum Institute of India (SII), a top European drug official has claimed that the vaccine is not even ready for conditional approval at the moment.

"They haven't even submitted an application to us yet," Wathion was quoted as saying in the report.

The UK aims to start rolling out the British AstraZeneca/Oxford vaccine from January 4.

According to Wathion, "The data we have at the moment is not even enough to give the AstraZeneca vaccine a conditional authorization".

"We need additional data about the quality of the vaccine. And after that, the company has to formally apply," Wathion added.

"We have 40-50 million doses of Covishield stockpiled. Once we get regulatory approvals in a few days, it will be down to the government to decide how much they can take and how fast. We will be producing around 300 million doses by July 2021," Serum Institute CEO Adar Poonawalla said during a press conference.

India currently has eight Covid-19 vaccine candidates, including three indigenous vaccines, under different stages of clinical trials which could be ready for authorization in near future.

Serum Institute-Oxford's Covishield, Bharat Biotech's Covaxin and Pfizer vaccines are in the fray for emergency use authorization.

The central government plans to vaccinate nearly 30 crore people in the first phase of the drive. It will be offered to one crore healthcare workers, along with 2 crore frontline and essential workers and 27 crores elderly, mostly above the age of 50 years with comorbidities.

Two days of dry run for the vaccination process was also successfully carried out in four states.

(This story was published from a syndicated feed. Only the headline and picture has been edited by FIT)