Manual drug product filtration system
Products
Information
The Cytiva™ manual drug product filtration system performs the sterile filtration of drug product. The system is designed to support the EU GMP Annex 1: Manufacture of sterile medicinal products by manually performing pre-use post sterilization integrity testing (PUPSIT) of the sterilizing-grade filters.
Minimize sterility breach with flow kits tested before and after sterile filtration of drug product.
Reduce time to implementation with ready-to-order standardized hardware and flow kits.
Movable valves accommodate a wide variety of single-use filtration flow kits with different filter sizes and configurations.
Economic, simple, and compact design.
