Social and facility assessment
SMETA / amfori BSCI assessment records, WRAP or equivalent facility reports when held by the shortlisted site.
Buyer due diligence
Share the product, destination market, and buyer standard first. We then align shortlisted capacity, evidence scope, inspection protocol, and commercial assumptions before quotation.

Qualification sequence
The compliance review is tied to the actual product, market, shortlisted site, and purchase-order conditions—not a generic certificate pack.
Product category, destination market, material claims, buyer standard, and delivery plan.
Match category capability, process scope, available evidence, and timing before disclosure.
Qualified buyers review scope-matched records through a controlled evidence workflow.
Testing, inspection, corrective action, fees, and release gates are recorded before bulk commitment.
Controlled evidence access
Full reports, supplier identities, worker data, and buyer-linked records are not published. After buyer qualification and NDA, available evidence is matched to the shortlisted program.
SMETA / amfori BSCI assessment records, WRAP or equivalent facility reports when held by the shortlisted site.
OEKO-TEX Standard 100 scope records, REACH / buyer RSL testing, and CPSIA support where applicable.
Redacted inspection samples, defect records, corrective-action status, and reinspection evidence where available.

QC protocol
The final sampling plan, defect catalogue, and release decision are agreed by product and PO. AQL is an acceptance-sampling method, not a defect-rate guarantee.
Destination-market support
The matrix describes testing and document support—not universal legal approval. Final obligations depend on product, material, market, economic-operator role, and contract.
REACH Annex XVII and buyer RSL test coordination; fibre, care, origin, and safety-document support where applicable.
FTC / Canadian textile and care-label support; CPSIA for children’s products and California Proposition 65 review when relevant.
OEKO-TEX scope checks, nominated laboratory protocols, retailer manuals, packaging rules, and buyer-defined restricted-substance lists.
Commercial terms
Final terms are confirmed after material, customization, evidence, testing, capacity, and destination review.
Next step
Send the product, destination market, quantity, material claims, buyer standard, and timing. We will identify evidence gaps and inspection requirements before commercial confirmation.