Every project operates under documented validation protocols, calibrated reference standards, and transparent data packets structured for regulatory review.
Analytical Testing
Quality Control Testing
Formulation Prototyping
Comprehensive chromatographic purity analysis, potency assays, and impurity identification utilizing HPLC and spectrophotometric detection for complex raw materials.
Routine batch release testing, stability storage studies, and quantitative contaminant screening aligned with standard compendial specifications and manufacturing timelines.
Bench-scale formulation development, solubility optimization, and emulsion stability testing tailored to regional cosmetic, nutritional, and specialty chemical manufacturers.
Instrumentation and protocol integrity
High-throughput chromatography
Our facility maintains calibrated UHPLC, GC-MS, and UV-Vis spectrophotometers. We calibrate every assay against verified reference materials to ensure unambiguous peak identification and reproducible compound quantification.
Verifiable chain of custody
From initial sample receipt to final certificate of analysis delivery, your compounds remain monitored under barcoded environmental logs, validated methods, and tamper-evident documentation systems.
Performance verified by data
99.8%
calibration repeatability rate
5 Days
standard assay turnaround
100%
bench-direct chemist communication
Maxel Labs resolved our raw ingredient potency variance within forty-eight hours. Their raw chromatographic data was clean, transparent, and immediately accepted by our audit team.
Dr. Marcus Vance, Director of Formulation QA
Having direct phone access to the analytical chemist running our stability chambers saved us weeks of email delays during our regional manufacturing scale-up.
Elena Rostova, Operations VP, Altaic Biotech