Characterisation, stability, bioactivity screening, formulation suitability and supply-chain comparability for novel and established functional ingredients. Useful when you need an independent, structured view on what an ingredient really is and how it behaves.
Identity, purity and marker-compound profiling for new ingredients
Comparability between batches, suppliers and country-of-origin
Bioactivity screening for functional and bioactive ingredients
Solubility, stability and formulation-suitability evaluation
Adulteration, substitution and economic-fraud screening
Provenance and supply-chain traceability supportive analytics
Specification design for new ingredients entering the supply base
Forced-degradation and stability liabilities mapping
Marker compound and active assay; potency profiling.
Untargeted screening, fingerprinting and structural confirmation.
Volatile profile and essential-oil characterisation.
Identity confirmation and qualitative comparison.
Elemental and heavy-metal profiling.
Structural confirmation for novel chemical entities.
Methods, documentation and acceptance criteria are designed to align with the standards below. This describes design intent — formal accreditations are listed on the About page.
Ingredient characterisation report with full data tables
Comparability assessment across batches and suppliers
Bioactivity screening summary
Specification draft for adoption into supply contracts
Adulteration / substitution investigation reports
Recommendation memo for sourcing decisions
Send a short scope and we'll come back with a quote and indicative timeline within one working day.