License Number: 91441900MA4WN5MJ8Y
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On-the-ground China sourcing since 2011
ISO 9001–certified and export-licensed. Audited factories, enforceable contracts, and on-site QC—turning specs into dependable production.
Quick Facts
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Founded: 2011 (Hong Kong, China Inter-Trade Alliance)
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China entity: Dongguan SHAMANA Trade Co., Ltd. (est. 2017)
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Location: Dongguan, Greater Bay Area (direct access to major supplier hubs)
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Facility: ~700 m² office & warehouse
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Compliance: ISO 9001:2015; Chinese export license; authorized for Class I & II medical devices
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Coverage: EU, Middle East, North America, South America, Africa.
What we believe
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Professionalism. Structured RFQs, clear BOMs, measurable acceptance criteria.
Integrity. We decline unsafe or non-compliant projects. No hidden commissions.
Safety. Contracts enforceable in China, traceable paperwork, safety culture on site.
Innovation, controlled. Pilot first, measure, then scale—no surprises.
How we work (4 stage-gates)
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Discover — specs, compliance, budgets, timeline, import country.
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Define — RFQ with 2–3 validated plants; samples; landed-cost scenarios.
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Pilot — small lot with IQC / First-Article / IPQC, CAPA loop, sign-off.
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Scale — volume with PSI, packaging audit, clean export documents.
Every step leaves evidence—photos, timestamps, reports.
Our timeline
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2011 — Inter-Trade (Hong Kong). Serving industrial buyers.
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2017 — SHAMANA China (Dongguan). ISO framework and local contract enforcement.
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2018–2023 — Operating system built. On-site QC, supplier audits, medical-device authorization, export/logistics playbooks.
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Today — End-to-end partner. From RFQ and factory validation to production, QC and legal exports.
Safety & QC
Safety is built into our daily routines—PPE on site, structured checklists, and four QC gates (IQC, First-Article, IPQC, PSI). We audit packaging and labeling to protect your product through last mile and customs.
Leadership & team
European-led, multilingual, China-based. Sourcing managers, auditors, QC engineers and PMs who bridge cultural and technical gaps—on the factory floor and in the boardroom.
Facility & footprint
Headquartered in Dongguan (GBA) with ~700 m² for sampling, secure storage and pre-shipment checks. Coordinated freight (sea/air/rail/multimodal) to EU, MENA and North America.
Proof & governance
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ISO 9001:2015 quality management system.
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Chinese Export License, details available on request.
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Medical devices authorization — Class I & II.
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Factory audits — legality, capacity, tooling, certificates (photo evidence & checklists).
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Contracts that work in China — specs, IP, acceptance criteria & penalties.
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On-site QC — IQC → IPQC → PSI, with CAPA when needed.
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Clean exports — traceable paperwork, predictable customs clearance.
Our brand & OEM manufacturing
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HOROMA is our established display brand, built inside SHAMANA’s operating system—the same audited factories, enforceable contracts, on-site QC and compliant exports that power our client work.
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Alongside HOROMA, we deliver OEM / private-label production for selected items under our clients’ brands, with evidence at every step.
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HOROMA displays — validated plants, on-site QC at four gates (IQC, FAI, IPQC, PSI).
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OEM/private label — industrialize to your spec, protect IP in China contracts, clean exports.
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Governance & compliance — ISO 9001, documented audits, traceable materials & packaging checks.
SHAMANA China Gallery
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Monthly China supply insights—standards updates, QC checklists, and new case studies.
Ready to start?
Start a pilot run — open production in a qualified plant, stabilize, then scale.
Or Upload your project and receive a structured brief within 1–2 business days.
Mini-FAQ
Q: Do you support OEM/private-label and your own brand?
Yes. We operate OEM/private-label programs for selected items and also manufacture HOROMA display solutions inside our audited supply chain. Both follow the same controls: enforceable China contracts, on-site QC at four gates, and compliant exports.
Q: How do you protect IP and commercial terms in China?
We use enforceable contracts (NNN + specs annexes, acceptance criteria, penalties), vendor NDAs, controlled document access and on-site oversight. Designs and tooling are handled with ownership clauses and traceable hand-offs. We decline projects that can’t meet our compliance bar.
Q: What MOQs and timelines should we expect?
We design for pilot-first, then scale. MOQs depend on process/tooling; we typically start with a small lot to stabilize quality, then move to volume. After RFQ validation, first pilot timing is set jointly with the plant; we share a dated Gantt with QC gates (IQC/FAI/IPQC/PSI).
Q: What compliance do you cover?
ISO 9001:2015 QMS, Chinese Export License, and authorization for Class I & II medical devices. We coordinate testing and documentation with the plant and accredited labs.
Q: Can you manage logistics and customs documents?
Yes. We prepare clean export paperwork, coordinate sea/air/rail or multimodal freight, and verify packaging/labeling. Incoterms are agreed up front; we provide photo evidence and time-stamped reports at each QC gate to de-risk clearance.
Q: What do you need from us to start a pilot?
A concise brief and basic company info: drawings/specs, standards, annual volume, target price range, destination country, preferred Incoterms, required certifications, and your legal details (company name, VAT/tax, bill-to/ship-to, contacts). We run a 24–48h scoping and propose validated plants and a pilot plan. Upload your project (link: /upload) or download our Client Data Sheet (link: /client-data-sheet.pdf).
