Six service lines, one quality system. Ask us about anything you don’t see here — we develop new methods every month.
Release and stability testing of APIs and finished products to pharmacopoeia methods.
HPLC, GC, dissolution, impurities and residual solvents to IP, BP, USP and EP.
Nutrition labelling, contaminants and shelf life for food and beverage brands.
Nutritional analysis, pesticide residues, mycotoxins, heavy metals and microbiology, reported to FSSAI requirements.
Composition, structure and failure analysis for polymers, metals and batteries.
XRD, SEM-EDS, thermal analysis and particle sizing, with an engineer to interpret every result.
New analytical methods, developed and validated to ICH Q2.
From feasibility to a validated method and transfer to your QC lab, usually within six weeks.
Long-term and accelerated studies in qualified, monitored chambers.
Twenty-four walk-in and reach-in chambers at all ICH conditions, with 24/7 monitoring and alarm.
A dedicated team for your formulation, process or materials project.
Full-time scientists working in your project, with weekly reports and your IP protected by contract.