FILTER INTEGRITY ANALYZER
CUSTOM MADE FOR PHARMACEUTICAL FILTRATION
Standard: ASTM F316
Test Range: 0.1-10 microns
Test Duration: 6-7 minutes
Precision: 0.1%
TECHNOLOGY
A Filter Integrity Analyzer (FIA) evaluates a filter’s integrity through methods such as bubble point, diffusive flow, or pressure decay. The pressure drop across a filter against the flow rate of fluid passing through is measured, assisting in assessing filter integrity by revealing changes in pressure drop with flow rate. Meeting the bubble point condition requires pressure to surpass the minimum bubble pressure, while the forward flow condition is satisfied by an acceptable pressure drop, and the water intrusion condition is achieved when the filter effectively repels water, indicating a well-functioning filter. Equipped with specialized instrumentation like pressure transducers and flow meters, FIAs offer rapid and accurate analysis, aiding product quality and regulatory compliance in pharmaceutical manufacturing.
APPLICATIONS
- Cross Flow/ Tangential Filter
- Syringe Filter
- Depth Filter
- Flat Sheet Membrane
- Capsule Filter
- Cartridge Filter
CUTTING EDGE DESIGN
SIMPLE | INTELLIGENT | MORE INTEGRATED
The hardware system has evolved into a highly sophisticated instrument with increased ease-of-operation, data accuracy, reliability, and end-to-end automated operation.
ADVANCED SOFTWARE
AI BASED | DYNAMIC REPORTS | EASY TO USED
Unprecedented visualization and collaboration using new M19 software control program and test report program. Experience the power of A.I based cognitive software control program that virtually eliminated user bias throughout the data acquisition process and data interpretation, redefining the way data is generated and consumed by your team.
HIGH PERFORMANCE COMPUTING
INCREASED PRECISION | ACCURACY | REPRODUCIBILITY
M19 instruments deploy cutting-edge ARM7 group of 32-bit RISC ARM processor cores licensed by ARM Holdings for microcontroller use, which not only enhances the precision of our analyzers but also ensures consistent, reliable results across all testing platforms. With our technology-centric approach, we strive to set a new standard for material characterization, promoting credibility and trust in every test conducted.
KEY FEATURES
Focus on Accuracy
Industry-specific customization in hardware and software
control increases data accuracy to a whole new level.
Increased Focus on Reproducibility
Retaining test recipes and parameters of samples
ensures greater reproducibility.
21 CFR Part 11 Compliant
The Advanced Software meets the technical requirements
of FDA regulations 21 CFR Part 11 Compliant.
Ease of Use
Intuitive Interface, Operating System Functionality and
Facilitating Effortless Interaction with users.
Comprehensive Service & Support
Access services are available to conduct installation,
calibration and validation on-site.
M19 Lab Services representatives offer factory or on-site
maintenance and repair services.
KEY BENEFITS
High Precision
Accurate detection of even the tiniest leaks in your filters.
Rapid Testing
Expedite your quality control process without
compromising accuracy.
User-Friendly
Intuitive interface for easy operation by both experts and
newcomers.
Real-Time Monitoring
Instantaneous feedback for immediate decision-making.
Versatility
Compatible with various filter types and sizes.
