Trusted by the world's leading scientific organizations
Unify CDS + MS outputs across every vendor into one governed view for faster review, drift detection, and investigation-ready reporting.
Build AI-ready analytical data without compromising compliance, traceability, or your systems of record.
Luma’s Analytical Science solution automatically captures, parses, and harmonizes chromatography and MS data directly from source systems. Multi-vendor CDS outputs are transformed into a unified, traceable data layer that supports faster review, comparison, and investigation—without brittle scripts or manual data handling.
Unify chromatography and MS data, surface trends across runs, and spin up reusable, submission-ready reports.
Secure capture and normalization across vendors so chromatography and MS data land in one harmonized layer—no more brittle glue code or manual file handling.
Apply schemas, bind methods/samples/lots, and generate decision views that make cross-run and cross-instrument comparisons straightforward.
Chromatograms, integration summaries, stability and impurity trends, and review-by-exception views that surface drift and anomalies fast.
Post results to your ELN maintaining full lineage, release signatures, and audit trails across methods, runs, and reports so experiments are reproducible and submission-ready.
Handle high-volume QC, analytical development, and purification data across instruments and sites with performance proven at enterprise scale.
Harmonized, contextualized data for modeling and AI-assisted guidance—without compromising compliance, traceability, or data integrity.
A global QC group harmonizes multi-vendor CDS outputs in Dotmatics, reviewing runs, methods, and lots in one view and accelerating lot release decisions.
Harmonizing CDS data for faster lot release
An analytical development team overlays chromatograms, trends stability and impurity metrics across runs and instruments, catching drift early and preventing costly OOS or repeat investigations.
Monitoring method performance to prevent drift and OOS
A late-stage biotech auto-generates reusable, traceable regulator-ready reports and supporting documentation from harmonized CDS data, standardizing deviation reports and CMC documentation while significantly reducing manual report-building effort.
Standardizing deviation reports and CMC documentation
