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Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice

This in-house capability has been a game-changer for lipolife, allowing us to take full control of formulation quality and consistency

[DOI] [PubMed] [Google Scholar] [83].Tao X, Yan M, Wang L, Zhou Y, Wang Z, Xia T, et al

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