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The FDA has recommended Ocugen Inc, the US partner of the Indian vaccine maker to go for the Biologics Licence Application (BLA) route with additional data which will delay the launch of Covaxin in the USA.

Explained: Why US FDA declined emergency use authorization to Covaxin?

Reviewing the vaccination status and availability in the state, the cabinet said it was necessary to source vaccines globally.

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Explained: Why US FDA declined emergency use authorization to Covaxin?

Vaccine Shortage: Punjab becomes first state to join global COVAX facility for procurement at best price