Application Note

Ensuring Homogeneity In Biopharmaceutical Aliquotation

SUS - homogenization

Biopharmaceutical production relies heavily on the homogeneity of pharmaceuticals. However, the varied viscosities and settling properties of liquid drugs make consistent aliquoting challenging. Manual homogenization can lead to contamination, uneven filling, and product quality reduction. A study conducted in partnership with the Medical University of Innsbruck demonstrated an automated approach to homogenizing biopharmaceuticals within single-use bags. The system ensured consistent cell counts across aliquots, eliminating the risks of manual handling.

The results, validated through statistical analysis, confirmed the effectiveness of this automated system in maintaining cell count consistency. This method not only improves patient safety by reducing deviations but also adheres to regulatory guidelines, ensuring reproducibility, and minimizing errors.

To delve deeper into the study's findings and the benefits of automated homogenization in biopharmaceutical production, access the full application note.

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