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Individual case reports of hormonal changes during treatment should be interpreted in the context of multiple contributing factors, including baseline hormonal status, concurrent medications, rate of weight loss, nutritional intake, and other medical conditions

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[9] Although this EMA guideline is written for synthetic peptides used in medicinal products rather than establishing mandatory specifications for all research-use materials, its distinction between identity, assay, peptide-related impurities, non-peptide impurities, and analytical controls is useful when interpreting a research-material COA

All investigations are performed in laboratory settings only