Four disciplines, one accountable process. We extract, standardise, test and trace every batch so that what is printed on the Certificate of Analysis is exactly what arrives at your dock — backed by in-house quality control and independent NABL-accredited verification.
Extraction
We extract with the solvent system that best preserves a botanical's target actives — water, hydro-ethanolic or solvent-based — and tune the drug-to-extract ratio (DER) to the concentration you need. Soft, dry and liquid forms are produced in-house, with spray-drying for free-flowing, stable powders.
Standardisation
Every standardised grade is locked to a defined marker-compound concentration and verified analytically — so the active percentage on the COA is the active percentage in the drum. We standardise to your target actives across documented grade ranges and confirm by validated methods.
Testing & QC
Material is screened in our own quality lab and cross-checked through third-party, NABL-accredited laboratories. We test identity, potency, contaminants and microbiology — and a Certificate of Analysis is issued for every single batch, never as a sample-only document.
Traceability
Each batch is lot-controlled and backed by complete batch records. Raw material is verified at source, and a full document trail follows the material from incoming inspection through processing to dispatch — so any lot you receive can be reconstructed end to end.
Each stage hands off to the next with documentation intact — no gaps between the field and the freight.
Send us your target marker, DER and contaminant limits. We’ll confirm feasibility, share representative documentation and outline a clear path to sample — within 24 hours.
