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Alicia Lundby, Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3, 2200 Copenhagen N, Denmark

Each batch undergoes quality validation including: analytical composition verification sterility testing endotoxin control screening stability consistency evaluation batch-to-batch reproducibility assessment Advanced laboratory systems ensure uniform concentration and structural stability across all production lots

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As a result, older patients are more likely to experience this temporary side effect