Testing a New Chromatography Column for Cleaning Effectiveness

Cleaning validation is a critical consideration in the pharmaceutical industry. Inadequate cleaning can result in contamination of drug products with bacteria, endotoxins, active pharmaceuticals from previous batch runs, and cleaning solution residues. Such contaminants must be reduced to safe levels, both for regulatory approval and to ensure patient safety.

Author(s):
Chris Antoniou , Hillary Carter
Journal:
BioPharm International, January 2006

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