Drug product filtration system

Drug product filtration system
Product Description

The Cytiva™ drug product filtration system operates using configurable recipe-controlled phases to automatically perform terminal sterilization prior to filling with maximum product recovery using standard flow kits. It has been designed to support EU GMP Annex 1: Manufacture of sterile medicinal products requirements for contamination control strategies with automated in situ pre-use post-sterilisation integrity testing (PUPSIT) and post-use integrity testing of sterile filters. Fully automated sterile filtration with configurable recipe-controlled phases Automated PUPSIT and post- use integrity testing Enhanced product recovery method for reduced product loss Compatible with a wide range of filter sizes Single-use flow kits for rapid turnaround between batches One system for both single and redundant filtration Integrated human machine interface (HMI)

Cytiva

  • Country/Region:
    United Kingdom
  • On CPHI since:
    2025

Cytiva

  • Country/Region:
    United Kingdom
  • On CPHI since:
    2025

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Cytiva resources (2)