Drug Product Filtration System (DPFS)

 

Category: Pharmaceutical

Exhibitor: CYTIVA

Booth No: L718

 

Characteristic

 

The Drug Product Filtration System complies with EU GMP Annex 1 for sterile medicinal product manufacturing. By incorporating automated PUPSIT and in-process filter integrity testing, the system supports a robust contamination control strategy. Utilizing single-use technology, it eliminates the need for CIP/SIP cleaning validation, reducing maintenance costs and shortening batch changeover time—ultimately enhancing production efficiency.

Key Features:
＊ Automated filter integrity and leak testing: Fully compliant with EU GMP Annex 1 PUPSIT requirements.
＊ Process consistency: User-programmable methods ensure batch-to-batch reproducibility.
＊ Easy single-use flow path installation: Step-by-step HMI guidance and clearly labeled flow paths simplify setup and prevent installation errors.
＊ Flexible filter compatibility: Supports a wide range of filter sizes—from small KA1 filters to standard 10-inch filters—accommodating various process scales.
＊ Enhanced product recovery: Patented recovery method minimizes product loss, maximizing yield.

 

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