LABORATORY

Integrity Testing

In the pharmaceutical industry, integrity testing of sterilizing filters is a fundamental requirement for critical process filtration. Compliance with FDA Guidelines is crucial, as filters used in sterile solutions like LVPs and SVPs must undergo integrity testing. Documentation of testing is essential and must be included in batch product records.

High flow capacity Reduced housing footprint and fewer cartridges.

Reliable retention Consistent performance across critical processes.

Broad compatibility Multiple media and seal configurations available.

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PRODUCT OVERVIEW

Designed for efficient, dependable filtration

Integrity testing in Australia is classified into two types: destructive and non-destructive. At CoPure, we prioritize quality assurance by conducting destructive testing on samples from every manufacturing lot of sterilizing-grade filter products. Additionally, non-destructive testing is performed on each sterilizing-grade filter before sale to ensure its integrity. ● Pre-Analysis Protection: Extends the lifespan of your HPLC columns by removing damaging micro-particles. ● High Flow Rates: Engineered with premium membranes for faster filtration with less hand pressure. ● Low Hold-Up Volume: Minimizes sample loss, making them ideal for high-value or limited-volume samples. ● Universal Compatibility: Available in multiple pore sizes and materials (like Nylon, PTFE, and PVDF) to suit any solvent.

Typical applications

Biopharmaceutical processing

Water and utility filtration

Industrial process fluids

Food and beverage

Integrity Testing

Designed for efficient, dependable filtration

Typical applications

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