There is no way one human has the technical, management, or mental capacity to consider, evaluate, prioritize, and make go/no-go decisions on all FDA foods, medicines, medical devices, vaccines and other products. I don’t care how much their staff “pre processes” the information.

Leronlimab is going to fall to the bottom third of a long list of a bottle-necked process. This is the equivalent of taking a sharpie to the weather map - with more lives at stake.