Supplement Export Documentation & Logistics
Global shipping with full compliance documentation.
Export Logistics and Documentation
IN-HOUSE CAPABILITY
Getting product out of the factory is only half the job. The other half is making sure the paperwork, the marking and the case packs match what your market and your freight forwarder actually need.
- Handled by our own team in Zhengzhou, not brokered out
- Documented at every step and released against a written specification
Manufactured under cGMP (SGS-audited, CN26/00005718), HACCP, ISO 22000 and HALAL systems across two GMP-certified in-house factories, with US FDA facility registration (18854076080) and a Chinese food production licence (SC11341018200838).
A supplement shipment that is correctly manufactured can still stall at a border if the paperwork is wrong. Documentation is therefore part of the production plan, prepared in parallel with the batch rather than assembled after it.
Documents Issued Per Shipment
- Commercial invoice and packing list
- Certificate of Analysis (COA) for the batch
- Material Safety Data Sheet (MSDS)
- Certificate of origin
- Health certificate, for markets that require one
- Specification sheet, nutritional panel and allergen statement
Shipping and Terms
| Item | Detail |
|---|---|
| Incoterms | EXW, FOB, CIF and DDP quoted on request |
| Loading | Cartons on pallets, container loading supervised and photographed |
| Modes | Sea freight, air freight and express consignment |
| Marking | Neutral or branded outer cartons, as your market requires |
| Tracking | Batch and shipping documents forwarded as they are issued |
Case packs and pallet configuration are agreed before production, shipping marks are applied to your specification, and documents are issued ahead of collection rather than after it.
Markets We Ship To
Our products go to more than 100 export markets. Requirements differ sharply between them — the United States, the European Union, the United Kingdom, the Middle East and South East Asia each have their own labelling and registration expectations, and the documentation set is adjusted accordingly.
What We Cannot Do For You
We can prepare the product, the label and the documentation. We cannot act as your importer of record, and we cannot register a product in your name in your own market — that step needs a local entity. See regulatory and registration support for what we can and cannot cover.
Everything Under One Contract
Formulation
Your formula or target actives turned into a stable, manufacturable specification.
Manufacturing
Blending, encapsulation, compression, gummy depositing, powder and liquid filling.
Quality Control
In-process checks and finished-product release testing against the written spec.
Documentation
Batch records, a Certificate of Analysis and export paperwork with every shipment.
Plan Your First Shipment
Share the destination port, the volumes and the pack formats. We reply within 48 hours with a logistics view and indicative timing.