PURfect P^® Software

PURfect P® integrates a DOE experimental design module, enabling intelligent screening of the optimal purification process through minimal experimental iterations. As a domestically developed software with full intellectual property rights, it is compliant with FDA 21 CFR, GLP, and GMP pharmaceutical regulations, providing complete process logging and data traceability. It features multiple alarm protections for pressure, bubbles, and fraction collection, with automatic data archiving to prevent data loss from power outages. WiFi-enabled remote monitoring via mobile devices allows cross-workstation supervision of experiments, making it a highly stable, integrated chromatography data management platform.

Product Description

The brand‑new PURfect P^® software perfectly integrates DOE function. Via intelligent optimization, the DOE provides optimum experimental settings and results from minimum experimental runs.

‑ Developed independently with proprietary intellectual property, focusing on Chinese customers.

‑ Compliant with FDA 21 CFR/GLP/GMP and other relevant regulations, meeting the pharmaceutical industry's requirements for data traceability and integrity.

‑ A powerful, advanced, and highly stable chromatographic data management system.

‑ Full‑process LOGBOOK recording, with protection features such as pressure alarms, collection alarms, and bubble monitoring to safeguard the chromatographic column and samples in real‑time.

‑ Data are automatically saved in real‑time to prevent data loss due to unexpected power outages.

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