Quality & compliance

You can't audit a promise. You can audit a COA.

Anyone can say their extract is clean. What matters to your QA team is which method was used, what the limit was, and whether the number sits inside it. Here is exactly what we test, how, and how often.

In-process control

Quality control parameters

Five checks run on every single batch. The rest run on a defined frequency, and always ahead of an export consignment.

In-process and release testing. Product-specific ranges are agreed in the specification before production.
Parameter Method Specification Frequency
Appearance & colour Visual inspection Clear to slightly turbid; product-specific colour Every batch
Refractive index Abbe refractometer Product-specific RI range Every batch
Specific gravity Hydrometer / density bottle Product-specific SG range Every batch
Moisture content Karl Fischer titration < 0.5% Every batch
Extraction yield Extract weight / raw material charged × 100 Ginger ≥ 5.5%; product-specific Every batch
Active content (e.g. gingerols) HPLC ≥ 20% total gingerols for ginger extract Weekly, or on customer request
Heavy metals (Pb, Hg, As, Cd) ICP-MS Within EU / USFDA limits Monthly and on every export shipment
Microbial count (TPC, E. coli, Salmonella) Standard microbiological methods As per FSSAI / FCC / EP standards Monthly
Residual CO₂ solvent Headspace GC < 0.1% (food-safe threshold) Every 10th batch
Pesticide residues Multi-residue GC-MS Compliant with EU MRL limits Quarterly and on every export shipment
Certificate of Analysis All parameters above Full COA issued with the consignment Every batch
Need a parameter that isn't on this list — an ICH residual solvent panel, a specific allergen declaration, an EP or USP monograph assay? Tell us at enquiry stage and we'll confirm whether we run it in-house or through our accredited partner lab.

In the lab

What sits behind the numbers

Our in-house lab handles routine release testing — physical parameters, moisture, yield and identity. Instrumental work that requires accreditation for export documentation goes to a NABL-accredited partner laboratory, so the certificate carries third-party weight where your market needs it.

The QA function reports to the partners, not to production. That's deliberate: the person who can hold a batch shouldn't report to the person whose numbers depend on releasing it.

In-house

  • Physical parameters
  • Karl Fischer moisture
  • Yield reconciliation
  • Identity & sensory
  • Retained samples

Accredited partner lab

  • HPLC assay
  • GC-MS profile
  • ICP-MS heavy metals
  • Pesticide residue panel
  • Microbiology

Certifications & registrations

Certified to manufacture, accredited to test

Licences and certificates are held at the plant and copies go out with supplier qualification packs. If your procurement team needs a specific certificate, scope statement or audit report, ask and we will send it.

FSSAI

FSSAI Manufacturing Licence

Food Safety & Standards Authority of India

Licence no.

ISO
22000

ISO 22000:2018

Food Safety Management System

Certificate no.

HACCP

HACCP

Hazard Analysis & Critical Control Points

Certificate no.

NABL

NABL-Accredited Testing

Instrumental analysis through an accredited partner laboratory

Third-party validated COA

MSME

Udyam / MSME

Ministry of Micro, Small & Medium Enterprises — manufacturing enterprise

UDYAM-MH-30-0199739

GST

GST Registration

Goods & Services Tax Network — regular registration

27AAZFT2418G1ZQ

LLP

LLP Registration

Ministry of Corporate Affairs

LLPIN ACT-5607

AUDIT

Open to Audit

Batch records, calibration files and analytical data available for buyer and third-party review

By appointment

Working to a market that needs something we have not listed — Halal, Kosher, organic certification under NPOP or USDA NOP, or a customer-specific standard? Tell us at enquiry stage and we will confirm what we can supply against it.

Traceability

Back to the lot, back to the field

Batch identity

Every batch carries a unique number tying it to the raw material lot, extraction parameters, operator, date and analytical results. Retained samples are held against every batch.

Raw material lot

Incoming material is logged against supplier, region and season. Where we buy through FPOs and cooperatives, that traces back further than a broker purchase ever could.

Audit access

Buyers and third-party auditors are welcome at the plant. Batch records, calibration records and analytical files are available for review as part of your qualification process.

Send us your specification.

If you have a standard spec sheet or a supplier qualification questionnaire, send it across. We'll fill it in properly and tell you where we can and can't meet it.