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Sending it to FDA for review is like placing a bet.

$Novavax (NVAX.US)$
What I'm more concerned about is that FDA has already fully approved BNT and Moderna. Now, what needs to be passed is not the emergency authorization part, but what NVAX is submitting is the emergency authorization, so it's not just about having a response to Omicron. There are also updated variants of BA2, all of which require data and time for validation. It took at least a year for BNT and Moderna to go from emergency authorization to official approval. Do you think FDA will easily let NVAX pass? Or will additional documents be required? Hopefully, it's not just for the sake of submitting a document. It's worth everyone's attention.
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