We manufacture high-purity active pharmaceutical ingredients under controlled, fully documented processes. Every campaign is supported by validated analytical methods, defined impurity limits and the regulatory paperwork your filing needs — so the material that reaches your formulation team is predictable batch after batch.
Advanced intermediates and key starting materials supplied at consistent quality from kilo-lab through to commercial campaigns. We take on the steps that are difficult to run reliably in-house — and hold the specification that your downstream chemistry depends on.
An integrated CRAMS engagement gives you one accountable partner across the lifecycle: route selection and feasibility, process development and optimisation, scale-up and validation, and dedicated commercial capacity. Your IP stays yours — confidentiality and exclusivity are written into the engagement from day one.
Specialty and performance chemicals for pharmaceutical, agrochemical and industrial applications — produced to your specification rather than to a catalogue average. Where a standard grade does not fit your process, we will develop the grade that does.
Characterised impurities, degradation products, metabolites and reference standards with full structural elucidation and certificates of analysis. We isolate, synthesise and characterise the compounds your method validation and regulatory submission require — including the ones that are not commercially available anywhere.
You share the compound, specification, quantity and timeline.
Our chemists assess the route, cost and lead time, then quote.
Lab confirmation, sample supply and process optimisation.
Scale-up, validation and repeatable commercial delivery.
Send the compound name or CAS number, the quantity and the purity you need — we will come back with feasibility, lead time and pricing.