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However, these are merely early signals, and robust finding regarding efficacy cannot be made until the results of larger randomized controlled trials with determining endpoints come about

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The CoA should list the product name and full sequence, lot number, molecular formula, molecular weight, HPLC chromatogram with explicit percent purity, mass spectrometry identity confirmation (expected [M+H]+ at m/z 814.9), Karl Fischer water content, acetate counter-ion content, appearance, manufacture date, retest date, and the signature of the quality-control analyst