From first-in-class discovery to scale-up and regulatory filing — chemistry delivered with full documentation, transparency, and scientific depth.
We act as a seamless extension of your discovery team. From rapid analog synthesis to focused SAR library construction, our team brings speed and scientific rigor to your lead optimization campaigns.
From early route scouting to manufacturing readiness — our process chemistry team develops robust, cost-effective routes with full regulatory documentation and scale awareness built in from day one.
We synthesize and characterise pharmaceutical impurities and reference standards for IND, NDA, and ANDA submissions. Full ICH Q3A/Q3B compliance with traceable chain of custody and detailed analytical documentation.
Flexible, NDA-ready custom synthesis for any stage of drug development. Two engagement models designed to fit your program's structure — from single-compound requests to sustained multi-year programs.
Chemistry type, scale, timelines, and deliverable format — structured for program planning.
| Chemistry Type | Scale | Timeline | Key Deliverable |
|---|---|---|---|
| Heterocyclic analog synthesis | mg - kg | 2–6 weeks | Compound + CoA + NMR |
| Focused SAR library (5–50 compounds) | mg - g | 4–12 weeks | Library + data table |
| Complex natural product analogs | mg - kg | 6–16 weeks | Compound + synthesis report |
| Process route development | mg - g | 8–20 weeks | Optimised route + process report |
| Impurity reference standard | mg - g | 3–10 weeks | Certified standard + CoA |
| Degradation product synthesis | mg - g | 2–8 weeks | Compound + structural confirmation |
| Genotoxic impurity (ICH M7) | mg - g | 4–10 weeks | Certified GTI standard |
| Custom FTE synthesis program | Any scale | Ongoing | Milestone-based deliverables |
Send us your target structure, desired quantity, and timeline — we'll respond within 24 hours with a practical proposal.