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> I’d have directed an institute to run a report on theoretic safety and then a trial on volunteers.

Commonly known as “pre-clinical development” and “clinical trials”




Except you can skip steps because volunteers have already tested the vaccine for safety and at the end of the story there’s a vaccine that you can make as much as you want of. Instead of a vaccine controlled by a single company that, surprise surprise, has production issues that according to them surely can’t be overcome by using production capacity at other facilities.




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