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There is a deeper irony embedded in this practice: If buyers believed these products were safe, properly characterized and manufactured to the standards expected of pharmaceutical-grade products, they would not need to commission independent purity tests

These limitations do not invalidate preclinical findings but emphasize the need for human clinical trials with appropriate sample sizes, standardized protocols, and validated outcome measures before establishing clinical efficacy in human patients

This means more potent and direct effectiveness, which cant be matched by other delivery methods

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not safety/efficacy guidance