M19 Liquid Permeability Analyzer (LP-100) for pharmaceutical — AI-based, ultra-high-precision testing. Standards: REF. ISO 7231:2023.
Frequently asked questions
What does the LP-100 measure?
It characterizes liquid transport through pharma filter media: Liquid permeability / flux at controlled pressure Flow-vs-pressure behavior of membranes Comparative performance across media lots Inputs for membrane and process design
How does it outperform conventional flux tests?
Precise pressure control and accurate flow measurement give reproducible permeability values across low and high flux, with non-destructive testing suited to both R&D and QC.
How does the MFC-based approach improve accuracy?
The precision flow/pressure system: Maintains a stable differential across the specimen Measures flow with high resolution Reduces variability versus timed-volume methods Auto-calibrates for consistent results
What are the advantages of domestic manufacturing?
Local build delivers: Faster service and local support Reduced lead time and spare-parts availability Lower import cost and easy upgrades 2-year warranty with on-site support
Can it integrate into pharma workflows?
Yes — USB/Ethernet/SCADA connectivity, PDF/CSV reporting and 21 CFR Part 11 records let permeability data feed membrane development, QA/QC and validation.
How does it support regulatory compliance?
Referenced to ISO 7231:2023, with 21 CFR Part 11 electronic records and IQ/OQ/PQ documentation, the LP-100 keeps filter-development data audit-ready for US FDA, EU GMP and WHO GMP.