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Category: cleaning validation

  • Use of Non-Specific Methods Like TOC for Cleaning Validation

    For the effective removal of residues, Pharmaceutical and biopharmaceutical manufacturers, who perform manual, automated, or CIP (Cleaning in Place) methods of their production equipments are required to comply with regulatory requirements. To carry out this task, they perform various tests i.e. testing rinse water, cleaning water samples to ensure their cleaning process removes residues to […]