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In addition to these, NewBioRx applies stringent QA/QC systems with lot-level testing, traceability, and documented analytical specifications, aligning with established molecular reagent quality standards and reproducibility requirements
Here is a summary of the safety and tolerability data obtained from one of the two human clinical trials in which Fragment 176-191 was administered via I.V
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10.4049/jimmunol.1003032 [DOI] [PubMed] [Google Scholar] 96.Lokhorst HM, Plesner T, Laubach JP, Nahi H, Gimsing P, Hansson M, et al
