Four disciplines, one accountable process. We extract, standardise, test and trace every batch — and back it with the quality systems and documentation you can verify on paper. What is printed on the Certificate of Analysis is exactly what arrives at your dock.
Standardised potencies, controlled extraction ratios and a full test panel — visualised, then certified on paper.
Documented
HPLC, GC, HPTLC & UV marker quantification on standardised grades — never sample-only.
Standardised
Concentrated
A gentle, full-spectrum concentration.
Tested
In-house QC, cross-checked by independent third-party labs.
Extraction, standardisation, testing and traceability — auto-rotating every few seconds, or use the arrows to explore each.
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.
Each stage hands off to the next with documentation intact — no gaps between the field and the freight.
01Sourcing
Verified raw material at source
02Extraction
Solvent / water / hydro-ethanolic
03Standardisation
Marker compound to target %
04QC Testing
In-house + independent 3rd-party
05Packaging
Lot-coded, food-grade
06Export
Full document trail
We choose the extraction system that best preserves a botanical’s target actives — and tune the drug-to-extract ratio to the concentration you need.
Best for
Polar, water-soluble actives
Gentle, solvent-free extraction for polar compounds (e.g. many polysaccharides and glycosides). No residual-solvent concern; ideal where a clean, food-friendly profile matters.
Best for
Broad-spectrum standardised extracts
A tuned water–ethanol ratio pulls both polar and moderately non-polar actives — the workhorse for most standardised marker grades. Ethanol is recovered and residuals controlled.
Best for
Specific lipophilic markers / high purity
Selected solvent systems concentrate a target marker to high purity (e.g. 95% grades). Residual-solvent levels are screened and controlled to the limits of your market.
Best for
Volatile & lipophilic actives
CO₂ under pressure behaves as a tunable solvent for volatile oils and lipophilic actives, then leaves no residue as it returns to gas — a clean profile for sensitive compounds.
Whichever method applies, the marker % on the Certificate of Analysis is confirmed by validated analytical methods on every batch.
Our own extraction facility, quality-control laboratory and raw-material warehouse — the people and processes behind every batch we ship.
The systems, testing and paperwork behind every shipment — rotating through what we operate under and what each order includes.
Food-grade licence from FSSAI, India.
Ready for Gulf & Muslim-majority markets.
Registered for agri-product exports.
HPLC/GC/HPTLC marker COA on every batch.
We hold IEC, FSSAI, Halal and APEDA registrations, shared directly with serious buyers on request — so your QA team gets exactly what it needs to vet us.
International trade code (DGFT, India).
Food-grade licence (FSSAI, India).
Gulf & Muslim-majority markets.
Agri-export registration (India).
Our manufacturing network
Beyond our own licences, we manufacture through a vetted network of partner facilities — including GMP- and ISO-certified units — engaged as each order requires. Rather than overstate what we hold in-house, we place your product with a facility that already carries the exact certification your market demands.
Browse the document library, or have a specific document emailed straight to you. All certification claims are confirmed with documentary proof before an order is placed.
Have a spec?
Send us your target marker, DER, contaminant limits and destination market. We’ll confirm feasibility, which certifications apply, and a clear path to sample — within 24 hours.
