Quality & Compliance

Regulated-grade processes, traceable supply chains and audit-ready documentation — built to meet pharma, food and EU clean-label expectations.

Our Quality Pillars

We operate under documented ISO systems with a combination of in-house and accredited third-party testing (GC / GC-MS) and C-14 compliance readiness. COAs are issued per batch and provided to qualified buyers.

Quality Workflow (summary)

Raw material acceptance
Traceability checks
In-process QC (GC)
Final GC/GC-MS
COA issuance

Analytical & Spec Highlights

ParameterMansa Nutri — Natural CitralTypical Test
Purity≥85% (avg. ~87.1%)GC area %
Solvent ResidueNot detected / solvent-freeGC / Residue analysis
Residual PesticidesValidated below method LOQLC-MS/MS
MicrobialCompliant with pharma handlingPlate counts / specific tests
Radiocarbon (C-14)~100% pMC (consistent with plant origin; compliance ready)AMS / Radiocarbon test

COAs, GC/GC-MS reports and radiocarbon documentation are provided to qualified buyers under NDA or per order requirements.

Verified Documentation & Testing

Batch COA

Full COA available on request — includes GC summary, impurities, and packaging details. Provided per batch to qualified buyers.

GC / GC-MS Reports

GC/GC-MS chromatograms and method details are shared with qualified buyers; testing performed in-house and with accredited third-party labs as appropriate.

C-14 / Origin Validation

Radiocarbon tests are supported per order — Mansa Nutri material is C-14 compliance ready and can be validated through accredited AMS providers as requested.

Supply Assurance & Packaging

MOQ, lead time and pharma-grade packaging (20 kg / 200 kg drums) are confirmed at enquiry. Export documentation, handling protocols and required QA paperwork are provided for regulated markets.

Frequently Asked Questions

How do you verify natural origin?

Each production batch is supported by GC/GC-MS analytical data. Material is C-14 compliance ready and can be validated through accredited radiocarbon (AMS) labs upon buyer request.

Are samples accompanied by COA?

Yes. Samples include a summary COA with key assay and purity. Full reports (GC/GC-MS) are shared with qualified buyers on request.

What purity specification do you guarantee?

Guaranteed minimum: 85% purity. Typical batches average ~87.1%.

Do you perform the C-14 test in-house?

No. We are C-14 compliance ready and coordinate testing with accredited third-party labs as required.

Can you support pharma-grade packaging?

Yes — pharma-grade drums (20 / 200 kg) and QA documentation are available for qualified orders.

Last updated: 2025. For technical discussions and specific test requests, contact our quality team via the contact page or the Request COA link above.