Streamline your research workflow with instrument data integration, automated version tracking, and regulatory-compliant documentation.
FDA 21 CFR Part 11, GxP, and ISO compliant documentation with audit trails and e-signatures.
Seamlessly capture data from analytical instruments, devices, and equipment in real-time.
Automatic versioning with complete history, timestamps, and change tracking for every entry.
Intelligent search, pattern recognition, and automated report generation to accelerate research.
Link your instruments and devices to automatically capture experimental data.
Create structured entries with rich media, protocols, and real-time collaboration.
Generate compliance-ready reports with complete audit trails and validation.
Join leading research institutions and pharmaceutical companies worldwide.