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BumRushDaShow

(172,073 posts)
9. Correct
Thu Aug 19, 2021, 09:44 AM
Aug 2021

I think this is their way of "setting a deadline" so COVID-19 business is put at the front of the line, plus I know they give the bosses their time estimates/assessments on completion.

And from what I understand regarding both CDC's ACIP and FDA's VRBPAC, they have basically declared "all hands on deck" to get it done.

It's not just clinical stuff that is being looked at for the final approval but also the manufacturing processes (including sterility data and ascetic techniques, etc) and any last minute changes that the firms might have made since their last inspections to ensure that the batch testing is being done per SOP, etc.

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