Treat our laboratory as an extension of your own research group. From a brief feasibility study through a multi-month impurity isolation programme to chemistry outsourced in full, our chemists produce submission-grade work under signed confidentiality, tracked against weekly milestones and backed by complete spectral packages.
Innovator pharma, generic formulators, biotech start-ups and academic groups all use the same service: execution at the bench, analytical depth, and the regulatory documentation any serious research engagement demands.
Start a CRO ProjectLiterature survey, retrosynthetic analysis and feasibility benchwork to take the risk out of a target before a route is committed to.
Improving yield, cutting solvent, controlling impurities and tuning purity, all aimed at an untroubled move to commercial scale.
Isolation, synthesis and ICH-aligned characterisation of process, degradation and forced-degradation impurities.
HPLC, GC and LC-MS methods developed and validated to ICH Q2 expectations, documented ready for the dossier.
Stress testing across acid, base, oxidative, thermal and photolytic conditions, following ICH Q1A stability principles.
Submission-ready CoAs, NMR, Mass and IR spectra plus ICH Q3A/Q3B impurity profiles for filings in any market.
It is equally a project-management, communication and audit-trail exercise. We handle all four, which leaves your own people free for the work only they can do.