By allocating 21. 8B/year to a decentralized FDA, automating efficacy testing through pragmatic clinical trials integrated into standard healthcare, this clears the 443 years (95% CI: 324 years-712 years) treatment testing backlog in 36 years (95% CI: 11. 6 years-77. 2 years), delivering 637: 1 (95% CI: 569: 1-790: 1) ROI, saving 10. 7B deaths (95% CI: 7. 39B deaths-16. 2B deaths), and generating 58. 6B (95% CI: 49. 2B-73. 1B) in annual R&D savings at 0. 841 (95% CI: 0. 242-1. 75) /DALY (97. 7% (95% CI: 97. 5%-98. 9%) cost reduction, 12. 3x (95% CI: 4. 19x-61. 3x) capacity increase).
Mike P. Sinn (Wed,) studied this question.
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