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Because research-grade material is not manufactured to sterile-injectable pharmaceutical standards, sterility and endotoxin content are not guaranteed by the supplier the way they would be for an approved parenteral drug a point that belongs squarely in the safety discussion below

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It is formed from hexahydroxydiphenic acid (HHDP) through oxidation of the plant hydrolysable tannins

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Our commitment to quality continues beyond there

specific tendinopathy), validated biomarkers and functional outcomes, long term safety and immunogenicity surveillance, and pharmacovigilance for angiogenesis related adverse events