From fragmentation to break-loose force: A complete USP <382> assessment in parenteral delivery systems

Download the whitepaper to discover the results of a comprehensive USP <382>-aligned evaluation conducted on a selection of industry-standard elastomeric components integrated into 3 ml ready-to-use cartridge systems filled with histidine buffer. The study included deterministic testing for fragmentation, Container Closure Integrity (CCI), liquid leakage, resealability and break-loose and gliding force, referencing the relevant ISO standards ISO 11608-3, ISO 21881 and USP <1207>.

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