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In practice, that covers: HPLC (high-performance liquid chromatography) purity testing on the active peptide prior to fill Sterility and bioburden checks on the finished cartridge Lot-number assignment tying the analytical results to the specific production run Specific purity percentages and endotoxin limits for the current batch should be confirmed with our QC team at the point of order rather than assumed from a generic specification sheet

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doi:10.2337/diabetes.52.4.910

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