Quantifying biology with lab‑grade precision
A compact measurement platform for in‑process analytics, stability testing, and QC—purpose-built for pharmaceutical and diagnostics workflows.
±0.1% CV
Repeatability across runs
21 CFR Part 11-ready
Audit trails & e-signatures
Sub-minute readouts
High-throughput compatible
Trusted by teams in pharma & diagnostics
Product
A bench-top analyzer built for regulated environments
Non-destructive measurement with robust calibration models and automated audit trails.
Assay-agnostic
Compatible with multiple modalities—spectral, impedance, and fluorescence add-ons.
Real-time analytics
Live trendlines, SPC, and alerts when CQAs drift out of spec.
Compliance
User roles, e-signatures, and immutable logs for 21 CFR Part 11 readiness.
"Quantica reduced our release testing time by 68% while improving repeatability."
Head of QC, Top-10 Pharma
"Integration took two days. Audit readiness checks passed on first attempt."
Director QA, CDMO
Applications
Where it shines
From formulation development to lot release.
Biologics
Protein aggregation, titer, viscosity.
Small molecules
Dissolution, impurity profiling.
Microbiology
Cell viability, contamination flags.
Stability
Accelerated + real-time stability monitoring.
Publications
Peer-reviewed evidence
Explore datasets, methods, and validations.