Nobody buys machines. They buy trust in a process.
// Nine steps, each one gating the next
- 01
Raw Botanical
Botanical raw material from Himalayan-foothill sourcing, received and lot-logged at intake.
- 02
Identification
Species and plant part identified at intake, before anything is processed.
- 03
Authentication
Identity confirmed against reference material — a misidentified botanical cannot be corrected downstream.
- 04
Extraction
Extracted on site — supercritical CO₂ on the 300L unit, or a method matched to the compound.
- 05
Purification
ArcoPure™ purification isolates the target active from the crude extract.
- 06
Standardization
The active is fixed to one exact, repeatable specification — not a naturally variable blend.
- 07
Analytical Verification
Each batch is assayed in the in-house lab against the fixed spec and a Certificate of Analysis is issued.
- 08
Packaging
Packed in-house on the same site — no toll manufacturer between steps.
- 09
Global Distribution
Shipped with COA and specification to formulators in India, the UK, the EU and Japan.
The order matters more than the equipment. Identification and authentication come before extraction, not after it, because a botanical misidentified at intake cannot be corrected downstream — every purity figure that followed would be measured against the wrong plant. Standardization then precedes analytical verification, so what gets tested is the finished specification rather than a hopeful average. Nine steps, each one gating the next: that sequence is what makes a batch repeatable rather than merely successful.
// Facility
Extraction, laboratory work, freeze-drying, packaging and liquid filling all sit on one site in Selaqui. That matters less as a boast than as a chain-of-custody argument: material is not handed to a toll manufacturer between steps, so there is no gap in the record where a specification could quietly drift. The 300L supercritical CO₂ unit and the in-house R&D lab share the same floor, which is why an analytical method can be matched to each compound instead of borrowed from a generic protocol.
Processing
Packaging
Liquid filling line
Annual capacity runs to 100 MT, and the site operates under GMP, FSSAI, ISO 9001, ISO 22000 and FSSC 22000. The practical consequence for a formulator is that pilot volumes and commercial volumes come off the same line under the same certifications — the specification does not change when the order size does.
// Ships with every batch
- Certificate of Analysis against the fixed specification
- Product specification sheet
- Technical and regulatory dossier on request
Arceli Lifescience