cant agree more...while the testing protocol is needed for approval, he clearly saw that it was working and wasted no time ( or lives) "for a p-value" - (remember that quote?)...dr jay says that the FDA and others "hated" the eIND process, so much paperwork....do you hate dying? maybe streamline the eIND process in a time of a pandemic level house-is-currently-on-fire emergency? over and over again it is apparent that the FDA does not treat any of this as an "emergency", just business as usual