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Responsible innovation, with clinical-grade evidence, privacy and equity designed in from the start, and tools built around real clinical pathways rather than bolted on afterwards, is not a brake on progress

and Herbert et al.s Research on Multivitamins circa 1980 While experiments by Kondo et al

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To run credible human RCTs you need GMP-grade material, stability data, sterility assurance, validated assays, and an approved clinical trial application