Supplier Verification in India: The Checklist Every Importer Should Use
The definitive supplier verification checklist for international importers sourcing from India — documentation gates, factory audit process, capacity and financial checks, certification verification, reference checks, trial orders, and a weighted risk scorecard with downloadable framework.
Supplier verification is the gate between a promising India RFQ and a supply chain that performs in your warehouse. India exported merchandise worth approximately **$441.78 billion in FY 2025–26** — but export readiness varies sharply among the MSMEs that form the manufacturing backbone. Two cumin processors quoting identical FOB prices may differ completely on Spices Board registration, steam sterilisation capacity, NABL laboratory access, and prior EU residue documentation. Verification separates capable export partners from polished directory listings.
International buyers, importers, distributors, and procurement managers who skip structured verification discover problems at destination customs — when demurrage, rejection, and rework costs are hardest to recover. Buyers who run documentation checks, factory audits, capacity validation, certification verification, reference checks, and trial orders before scale-up build supplier scorecards that compound trust across seasons.
This guide is the verification-focused companion to How to Find Reliable Suppliers in India and What International Buyers Look for Before Choosing an Indian Supplier. It provides an eight-step audit process, section-by-section verification checklists, a weighted supplier risk scorecard, trial order gates, and a **downloadable verification framework** you can use with your procurement team: Download Supplier Verification Framework (MD). For import mechanics through customs clearance, see The Complete Guide to Importing Products from India. Whether you verify factories directly or through a global sourcing partner in India, reliability is verified — not assumed.
Key Takeaways
- **Verification before deposit** — IEC, GSTIN, category licences, and sample export packs reviewed on government portals before samples ship.
- **Eight-step audit process** — credential pre-screen → documentation review → factory verification → capacity validation → certification check → references → sample approval → trial order with scorecard.
- **Factory verification is non-negotiable** — live video or on-site audit of production lines, QC stations, and category equipment; stock photos and showroom visits do not qualify.
- **Weighted risk scorecard** — minimum 70% score before trial order; 80%+ for scale-up without enhanced inspection.
- **Trial orders at partial container scale** validate documentation accuracy, PSI pass rates, and communication discipline before full programmes.
- **Download the framework** — Supplier Verification Framework includes checklists, scorecard template, audit report form, and red-flag list.
- Altus Exports pre-verifies manufacturers across spices, textiles, engineering goods, honey, and chemicals — collapsing verification cost for buyers without India staff.
Why Verification Matters
Verification is risk allocation at the point where procurement decisions are still reversible. When an international buyer wires an advance to an Indian supplier without structured checks, they are betting that licences are valid, the factory exists at the registered address, production capacity can sustain bulk volumes, export documentation will clear destination customs, and the counterparty will respond when certificates need reissue or pre-shipment inspection flags non-conformances. Each bet that fails costs more than the price delta between the lowest and second-lowest quotation.
The failure economics are brutal and often invisible in initial RFQ comparisons. Destination customs holds generate demurrage, storage, and broker fees that exceed margin on the shipment. Retail programme rejections after customs release trigger delisting conversations. Engineering buyers who receive non-conforming batches face line-stop costs that dwarf unit savings from an unverified low bidder. Procurement teams that treat verification as a structured process — not a courtesy call before payment — protect margin, compliance standing, and customer relationships simultaneously.
India's export depth amplifies both opportunity and variance. Regional clusters — Rajasthan and Gujarat for spices, Tamil Nadu for textiles, Punjab and Maharashtra for engineering — host genuine manufacturing capability alongside traders who present factory credentials they do not control. The **China+1 diversification trend** has accelerated buyer interest in India, but interest without verification produces the same failure patterns documented in 10 Common Mistakes International Buyers Make When Sourcing from India.
Practical example: a German food distributor evaluating coriander programmes received three quotations within eight percent on FOB. Supplier A shared IEC verified on DGFT, Spices Board registration, redacted EU export pack, and live video of sortex and steam lines. Supplier B sent a catalogue and promised "export quality." Supplier C quoted twelve percent below market. The buyer's verification workflow eliminated B and C before samples — not because product quality was tested yet, but because credential and documentation evidence predicted downstream customs and batch consistency risk. Supplier A's trial order cleared PSI at first attempt; the buyer scaled to full container programmes within two crop years.
Verification also compounds positively. Suppliers who pass structured audits and trial orders invest in export infrastructure when buyers provide consistent milestone communication, fair payment terms, and volume growth on positive scorecards. Buyers who re-auction every order on price alone restart verification cost and lose batch consistency. The best India sourcing relationships look boring: same specs, same documents, same milestones — season after season.
“Verification is not bureaucracy — it is the cheapest insurance in international trade. Every hour spent checking licences and walking a factory on video saves days of demurrage and weeks of customer complaints at destination.”
Common Supplier Risks
Understanding common supplier risks helps importers build verification workflows that address root causes — not symptoms discovered when containers sit at destination ports. The risks below reflect patterns observed across spice, textile, engineering, honey, and chemical export programmes. They are not arguments against sourcing India; they are arguments for running the checklists in this guide before the first deposit.
“The most expensive supplier is often the cheapest quote — because the savings disappear at customs, in the laboratory, or when your retail buyer rejects the lot. Verification catches those suppliers before money moves.”
Trader posing as manufacturer
Trading companies and brokers frequently present themselves as manufacturers on B2B marketplaces and LinkedIn. They may source from unverified third parties, mark up without quality accountability, and lack export licence control over documentation. Mitigation: verify IEC entity against factory address; request live video showing production in progress; ask who signs health certificates and whether the IEC holder is the producer.
Invalid or expired licences
FSSAI licences lapse; Spices Board registrations cover different product scopes; ISO certificates on marketing packs belong to unrelated facilities. Buyers who accept PDF copies without portal verification discover gaps at certificate application stage. Mitigation: check IEC on DGFT, GSTIN on GST portal, FSSAI on FoSCoS, and certification scope directly with issuing bodies.
Documentation nomenclature mismatch
A cumin shipment where the health certificate abbreviates product name differently from the retail label fails import broker matching at destination — even when spice quality is acceptable. Mitigation: review redacted export packs from prior shipments before order placement; align nomenclature across invoice, COA, phytosanitary, and health certificates in writing.
Capacity overcommitment
Factories that accept every order regardless of equipment availability miss sailing dates, subcontract to unverified units, or dilute quality during peak season. Mitigation: validate throughput, shift patterns, and honest peak-season communication during factory audit.
Sample bait-and-switch
Hand-prepared marketing samples that cannot be reproduced on bulk equipment are a recurring failure mode. Mitigation: require samples from production runs; retain signed reference samples; schedule pre-shipment inspection against approved specs.
Inspection and transparency refusal
Suppliers who reject third-party pre-shipment inspection, refuse factory video access, or pressure for 100% advance before samples signal reliability risk regardless of quoted price. Mitigation: treat these as automatic disqualifiers — see red-flag list in the downloadable framework.
Documentation Verification
Documentation verification is the fastest, lowest-cost gate in the supplier audit process — completable in days if the supplier is export-ready, and a reliable early disqualifier if credentials do not align. Every document check should confirm three things: the entity name matches across sources, the licence scope covers your product category, and sample export packs from prior shipments show nomenclature precision your destination market requires.
Start with **IEC (Import Export Code)** verification on the DGFT portal. The ten-digit IEC must be active, and the legal entity name must match the company presenting the quotation. Cross-check **GSTIN** on the GST portal — registered address should align with the factory location, not only a corporate office in another state. For companies, request **CIN** from MCA records or a recent incorporation document to confirm legal structure.
Category-specific licences form the next layer. Food and spice exporters need **FSSAI licence** verified on FoSCoS with product scope covering your SKU. Spice programmes require **Spices Board registration**. Scheduled agricultural products need **APEDA registration**. Textile exporters may hold **OEKO-TEX** or **GOTS** certificates. Chemical exporters need accurate **SDS** templates and batch **COA** formats. Never accept licence PDFs without portal or issuer verification — expired and mismatched certificates appear frequently on supplier marketing materials.
Request a **redacted export document set** from a prior shipment to a market similar to yours: commercial invoice, packing list, bill of lading extract, phytosanitary certificate, health certificate, fumigation certificate where applicable, and certificate of analysis. Review whether product descriptions match precisely across documents, whether the shipper on the B/L matches the IEC holder, and whether certificate timelines appear realistic for your production schedule.
Practical example: a UK retail buyer qualifying an organic honey supplier verified IEC and FSSAI on government portals, confirmed APEDA registration, and reviewed a redacted export pack from a prior EU shipment. The health certificate named a different legal entity than the IEC holder — revealing a trader intermediary. The buyer requested direct factory introduction, re-ran documentation verification against the processor's licences, and proceeded with a compliant programme. Discovery at RFQ stage cost two days; discovery at UK border would have cost weeks.
Full export documentation depth for shipment execution appears in our Export Documentation Checklist for India and phytosanitary and health certificates guide. The documentation verification checklist in the downloadable framework provides a tick-box format for procurement teams.
- **IEC** — active on DGFT; entity name matches quotation
- **GSTIN** — valid; address aligns with factory
- **FSSAI** — FoSCoS verification for food; scope covers SKU
- **Spices Board / APEDA** — category registration current
- **Sample export pack** — nomenclature aligned across invoice, COA, phyto, health
- **ISO / organic / OEKO-TEX** — scope verified with issuing body
Factory Verification
Factory verification confirms that production capability exists at the registered address, on equipment relevant to your SKU, with QC infrastructure that can sustain export programmes. Stock photos, showroom visits, and trade-fair booths do not substitute for observing active production lines, raw material storage, retention sample protocols, and category-specific equipment.
Buyers without India staff typically conduct **live video audits** — scheduled video calls where the supplier walks production areas in real time, shows equipment operating or ready for the relevant SKU, opens QC stations, and answers technical questions without scripted delays. On-site audits by the buyer, a third-party agency, or a find manufacturers in India partner provide stronger evidence for scale-up programmes.
“A factory audit is twenty minutes of video that saves twenty days of demurrage. Walk the production line, see the QC station, confirm the steam unit or the loom — then talk price.”
Eight-step supplier audit process
Use this sequence for every new supplier qualification. The downloadable framework includes a printable audit report template.
**Step 1 — Credential pre-screen (Week 1):** Verify IEC, GSTIN, and category licences on government portals. Disqualify if entity names mismatch or licences are expired.
**Step 2 — Documentation review (Week 1–2):** Review redacted export pack; confirm nomenclature alignment; map certificate timeline to your production schedule.
**Step 3 — Factory verification (Week 2–3):** Live video or on-site audit of production lines, QC stations, raw material storage, and export packing area.
**Step 4 — Capacity validation (Week 2–3):** Confirm equipment throughput, shift patterns, peak-season constraints, and subcontracting disclosure.
**Step 5 — Certification verification (Week 2–3):** Verify ISO, HACCP, organic, OEKO-TEX, or GOTS directly with issuing bodies; confirm scope covers producing entity.
**Step 6 — Reference checks (Week 3):** Contact export references or review redacted shipment history to similar destinations.
**Step 7 — Sample and lab approval (Week 3–6):** Approve bulk-equipment samples against written specifications; run destination-relevant laboratory panels.
**Step 8 — Trial order and scorecard (Week 6–16):** Execute partial-container trial; pass pre-shipment inspection; complete weighted scorecard before scale-up.
Minimum timeline: **eight weeks** for industrial SKUs; **sixteen weeks** for regulated food and spice programmes where lab panels and certificate lead times extend sample approval.
What to observe during factory audit
Spice processors: sortex lines, grinding equipment, steam sterilisation or approved treatment units, moisture-controlled storage, NABL or ISO 17025 laboratory access, export packing segregation from domestic lots.
Textile units: looms or cut-and-sew lines relevant to SKU, inline GSM or dimensional checks, dye house if applicable, OEKO-TEX handling procedures, carton packing for export.
Engineering factories: CNC or relevant machining lines, heat treatment capacity, dimensional inspection stations, material traceability, tooling storage for repeat programmes.
Honey processors: extraction and filtration lines, moisture testing, storage conditions, organic traceability if claimed, export labelling and packing area.
Across categories: confirm registered address matches facility, retention sample storage exists, QC sampling plan is documented, and subcontracting is disclosed if any process step is outsourced.
Factory audit red flags
Office-only meetings with no production access; reluctance to show equipment operating; facility address different from GSTIN registration without credible explanation; domestic-only packing area with no export segregation; inability to explain QC hold-and-release procedure; key process steps attributed to unnamed third parties.
Production Capacity Checks
Production capacity validation prevents a failure mode where a factory excels at trial volumes but cannot scale without subcontracting to unverified third parties or missing sailing dates during peak season. Capacity checks belong in the factory audit and should produce documented evidence — not verbal assurances.
Request visibility into **current order book** and realistic lead times from purchase order release to ex-factory dispatch. Ask about **shift patterns**, equipment relevant to your SKU, **backup power** if claimed, and **peak-season constraints** — Indian festival seasons and agricultural harvest windows tighten labour, freight, and processing slot availability across categories.
Category-specific capacity metrics matter. Spice processors need sortex throughput per day, grinder capacity, steam treatment slot availability, and storage conditions that preserve moisture limits across lots. Textile units need loom or cut-and-sew line capacity aligned to delivery windows. Engineering factories need machine availability, heat treatment capacity, and tooling locked for repeat programmes. Honey programmes need extraction throughput and lab testing slot coordination.
Ask the supplier to describe their **scale-up path** from trial order (pallet or LCL) to full container programmes. Honest communication about capacity ceilings scores higher than accepting every order and missing deadlines. Buyers often place trial orders at partial container scale specifically to observe whether production discipline holds when volume increases.
Practical example: a US hospitality buyer qualifying a Tamil Nadu towel manufacturer confirmed loom capacity, dye lot consistency protocol, and pre-Diwali production scheduling during video audit. The supplier disclosed a two-week capacity constraint before a major festival and proposed an ex-factory date that preserved sailing window — rather than accepting an impossible deadline. The buyer logged a positive capacity score on the supplier scorecard and allocated a repeat order after trial PSI passed.
- **Equipment throughput** — daily output relevant to SKU on production equipment
- **Lead time credibility** — PO release to ex-factory dispatch with milestone breakdown
- **Peak-season honesty** — festival, harvest, and freight constraints disclosed
- **Subcontracting disclosure** — any outsourced process step named and verifiable
- **Scale-up path** — trial pallet/LCL to full container without quality drift
Financial Stability Checks
Financial stability checks protect buyers from suppliers who accept deposits but lack working capital to procure raw materials, complete production, or survive a failed lot without disappearing. Financial verification is lighter than full credit analysis — but several practical signals predict counterparty reliability.
Review **export history** through redacted shipment documents, reference checks, and years in operation. A supplier with five years of consistent B/L history to your destination region carries lower abandonment risk than a newly registered entity with no export pack. Request **bank reference** or trade reference letters where programme scale warrants — especially for advance payments above your risk tolerance.
Evaluate **payment term alignment**. Excessive pressure for 100% advance before sample approval is a red flag. Standard structures include partial advance against proforma invoice, balance against copy documents, and letter of credit for large programmes. Suppliers who understand export finance and propose milestone-aligned terms often operate sustainable businesses; those who demand full prepayment for unverified first orders signal cash-flow desperation or fraud risk.
Assess **pricing sustainability**. Quotes far below market without process explanation suggest quality shortcuts, undisclosed subcontracting, or bait-and-switch after deposit. Model total landed cost — not FOB alone — when evaluating whether pricing is credible. A quotation ten percent below market that omits steam treatment, laboratory panels, or certificate fees often delivers higher total cost than a transparent all-in quote.
For scale programmes, consider **credit insurance** or **LC structures** that align payment release with document presentation. Merchant exporters and product sourcing companies in India who hold export licences and product title provide additional accountability layers when buyer financial exposure is significant.
Practical example: a Canadian distributor evaluating engineering component suppliers received a quote twenty percent below competitors. Documentation verification revealed IEC registered six months prior with no export pack available. Reference checks returned no verifiable destinations. The buyer disqualified on financial stability and transparency criteria despite attractive FOB — and later learned from an industry contact that the entity had failed to deliver on two prior advance-payment orders.
Quality Certifications
Quality certifications provide independent evidence that a supplier operates documented quality and compliance systems — but only when verified correctly. Buyers must confirm that certificate scope covers the **producing entity** and **product line**, that dates are current, and that claimed certifications map to destination market requirements.
**ISO 9001** demonstrates general quality management; **ISO 22000** and **HACCP** matter for food and spice programmes. **FSSAI licence** is baseline for food exports — verified on FoSCoS, not accepted from PDF alone. **Spices Board registration** and **APEDA registration** confirm category export authority. **Organic certifications** (NPOP, USDA Organic, EU organic) require scope verification and transaction certificate pathways on organic lines. **OEKO-TEX** and **GOTS** matter for textile programmes targeting EU and US retail.
Verification method: request certificate copies with scope pages, then confirm directly with issuing bodies or accreditation databases. Expired certificates, head-office ISO scope that does not cover the factory, and organic certificates for product categories outside scope appear frequently. Indian manufacturers who share scope pages proactively and renew before expiry avoid mid-season shipment pauses.
Certifications do not replace product testing. Buyers still require **bulk-equipment samples** approved against written specifications and **destination-relevant laboratory panels** — especially for spices (MRL compliance, ethylene oxide limits in EU), honey (antibiotic residues, HMF), and textiles (formaldehyde, azo dyes). See spice export quality testing and export certifications required in India for category depth.
Practical example: a Netherlands spice importer verified a supplier's ISO 22000 certificate and discovered scope covered warehousing only — not processing. The buyer required HACCP documentation for the processing line, re-audited the factory, and approved the supplier only after steam treatment and sortex operations appeared in an updated certification scope. Catching scope mismatch at verification saved a container hold in Rotterdam.
“A certificate on a website proves someone had a certificate once. Verification means checking scope, expiry, and whether the name on the certificate is the name on the IEC — today, for your product line.”
Reference Checks
Reference checks validate that a supplier has successfully executed export programmes — not only domestic sales or marketplace transactions. A supplier with credible export history to markets similar to yours has already navigated certificate workflows, inspection protocols, and nomenclature requirements your programme will face.
Request **two to three export references** — buyer company name, destination country, product category, and approximate shipment date. Contact references directly where possible. Ask whether documentation cleared customs without holds, whether pre-shipment inspection passed consistently, whether communication during production was reliable, and whether they would reorder.
Where direct reference contact is unavailable — common when suppliers protect buyer confidentiality — request **redacted shipment evidence**: B/L extracts with buyer names removed, certificate copies, and photos of export packing. Consistency across multiple shipments to the same destination region signals operational maturity.
Cross-check references against **trade data** and **sector council directories** where available. APEDA, Spices Board, and EEPC India maintain exporter listings that confirm registration status. Discrepancies between claimed export history and verifiable evidence warrant enhanced scrutiny or disqualification.
Practical example: a UAE food distributor qualifying a cumin supplier received three reference contacts. Two responded confirming repeat programmes and consistent certificate quality; the third reported a documentation nomenclature hold on one shipment that resolved in five days with supplier cooperation. The buyer weighted reference feedback positively — honest disclosure of a resolved issue scored higher than a supplier claiming zero problems across ten years.
Reference checks complement — not replace — documentation and factory verification. A supplier with strong references but expired FSSAI licence still fails credential gates. A supplier with perfect licences but no export history may be capable but requires enhanced trial order scrutiny.
Trial Orders
Trial orders are the final verification gate before full container programmes. They validate that approved samples reproduce on bulk equipment, that export documentation clears your import broker's pre-review, that pre-shipment inspection passes at agreed AQL thresholds, and that communication discipline holds under production pressure.
Size trial orders appropriately: **one pallet**, **LCL**, or **partial container** depending on category economics. Trial volume should be large enough to observe batch consistency and documentation workflow — but small enough to limit exposure if the supplier fails PSI or certificate accuracy checks. Spice and food programmes often trial at one to two pallets; textile programmes may trial at a few hundred units per SKU.
Before trial order release, confirm in writing: **signed specification sheet version**, **signed sample approval reference**, **payment milestones**, **incoterm and port**, **PSI agency and AQL thresholds**, **corrective action protocol**, **milestone reporting cadence**, and **certificate timeline** in the production schedule. Engage your import broker for draft document review before cargo dispatches — catching nomenclature errors at origin is far cheaper than at destination customs.
Trial order outcomes feed directly into the **supplier risk scorecard**. Pass PSI, clean documentation, on-time ex-factory dispatch, and responsive issue escalation produce scores that unlock scale-up. Failed PSI, certificate rework, or communication gaps during production produce conditional approval or rejection — regardless of sample quality at RFQ stage.
Practical example: a US retail buyer placed a one-pallet turmeric trial after scorecard score of seventy-eight percent. Pre-shipment inspection flagged moisture on one lot; supplier reworked before dispatch under agreed corrective action protocol. PSI passed on resubmission; documentation pack cleared US import broker pre-review. Buyer logged scorecard entry, reduced inspection intensity on repeat order, and scaled to full container within one crop year.
Trial order checklist appears in the downloadable framework. For full import workflow context, see What International Buyers Need to Know Before Importing from India.
“Trial orders are not a favour to the supplier — they are the buyer's last chance to verify reality before betting a full container. Treat them as a scored test, not a formality.”
Supplier Risk Scorecard
A weighted supplier risk scorecard converts qualitative verification findings into a comparable decision metric — enabling procurement teams to rank multiple suppliers consistently before trial orders and to log shipment performance for repeat-order decisions.
Score each criterion **1–5** (1 = unacceptable, 5 = excellent). Multiply by the weight below. Sum weighted scores and divide by five to produce a **percentage**. Use the same scorecard at qualification and after each shipment to track trends.
“Scorecards remove opinion from supplier selection. When three suppliers quote similar prices, the scorecard shows which one will actually clear customs — and that is the supplier worth a deposit.”
Scorecard decision thresholds
**≥80%** — Approve for scale-up; standard pre-shipment inspection intensity.
**70–79%** — Approve trial order; maintain enhanced PSI and milestone reporting.
**60–69%** — Conditional trial only; require corrective action on specific gaps before production release.
**Below 60%** — Do not place order; re-verify after gaps addressed or reject supplier.
After each shipment, log PSI outcome, documentation accuracy, lead-time performance, and communication quality. Two consecutive positive entries justify reduced inspection intensity; deteriorating trends trigger re-audit regardless of historical relationship.
Scorecard example — spice processor qualification
A UK buyer scored a Rajasthan cumin supplier: product quality systems 4 (20% = 16), documentation accuracy 5 (15% = 15), pricing transparency 4 (15% = 12), production capacity 4 (10% = 8), certifications 4 (10% = 8), communication 3 (10% = 6), lead times 4 (5% = 4), transparency 4 (5% = 4), compliance depth 5 (5% = 5), financial stability 4 (5% = 4). Total weighted: 82%. Decision: approve trial order with standard PSI; scale-up eligible after clean trial shipment.
- **Product quality systems (20%)** — sample quality, QC stations, lab pathway, retention samples
- **Documentation accuracy (15%)** — export pack review, nomenclature alignment, certificate timeline
- **Pricing transparency (15%)** — line-item quote, landed cost credibility, no hidden add-ons
- **Production capacity (10%)** — throughput validated, honest lead times, scale-up path
- **Certifications (10%)** — scope verified with issuing body, current dates
- **Communication (10%)** — response time, milestone reporting, issue escalation
- **Lead times (5%)** — credible schedule from PO to ex-factory
- **Transparency (5%)** — factory access, subcontracting disclosure, entity naming consistency
- **Compliance depth (5%)** — destination rules mapped, treatment and testing aligned
- **Financial stability (5%)** — export history, payment term reasonableness
Verification Checklist
Use this master checklist before placing your first purchase order with any new Indian supplier. Complete items in sequence — skipping steps inherits failure modes documented across our sourcing guides. For a printable tick-box version with audit report template, download the Supplier Verification Framework.
Related guides and next steps
Pair this checklist with How to Find Reliable Suppliers in India for supplier discovery channels, The Ultimate Guide to Sourcing Products from India for end-to-end sourcing workflow, and The Complete Guide to Importing Products from India for customs and landed cost depth.
Altus Exports supports international buyers with pre-verified manufacturer introductions, factory audit coordination, sample and production management, pre-shipment inspection, and export documentation aligned to major destination markets. **Download the framework, run the audit process, score the supplier, and trial before you scale** — that sequence protects every container that follows.
- **Credentials:** IEC verified on DGFT; GSTIN valid; CIN consistent; category licences current on government portals
- **Entity match:** Legal name consistent across IEC, GSTIN, quotation, and sample export pack
- **Export pack review:** Redacted prior shipment documents reviewed; nomenclature aligned across invoice, COA, phyto, health
- **Factory audit:** Live video or on-site audit completed; production lines and QC stations observed
- **Capacity:** Throughput, lead times, and peak-season constraints documented; subcontracting disclosed
- **Certifications:** ISO, HACCP, organic, OEKO-TEX verified with issuing body; scope covers product line
- **References:** Export references contacted or redacted shipment history reviewed
- **Samples:** Bulk-equipment samples approved against signed specification sheet
- **Lab testing:** Destination-relevant panels passed where regulations require
- **Commercial terms:** Payment milestones, incoterm, port, PSI agency, AQL, and corrective action protocol agreed in writing
- **Scorecard:** Weighted score ≥70% before trial order; ≥80% before scale-up without enhanced PSI
- **Trial order:** Partial container trial executed; PSI passed; documentation cleared import broker pre-review
- **Import readiness:** Landed cost modelled; import broker engaged; retention sample storage planned at destination
