Quality & Compliance
Supplements are regulated in most markets. We build quality control and documentation into every batch so your product is import-ready.
Batch-Level Quality Control
- Raw material inspection — active ingredients and excipients checked against specification and certificates
- In-process control — weight, hardness, disintegration and blend uniformity during production
- Finished product testing — assay, identity, purity and microbiological testing per batch
- Certificate of Analysis — issued with every batch, aligned to your market's labeling requirements
- Stability support — shelf-life and storage studies to support your registration and claims
- Documentation — batch records and compliance paperwork for your import process
FDA-Registered Establishment
Shaanxi Haiyue Shengda Trading Co., Ltd. holds a current US FDA facility registration, confirming our establishment is listed with the U.S. Food and Drug Administration.
| Legal Name | Shaanxi Haiyue Shengda Trading Co., Ltd. |
|---|---|
| FDA Registration No. | 11057149244 |
| D-U-N-S Number | 540239665 |
| Registered Address | Room 789, 6th Floor, Block C, Lanchi Building, Qinhan New City, Xixian New Area, Shaanxi Province, China |
| Registration Period | FY2026 (issued May 21, 2026 - expires December 31, 2026) |
Note: FDA facility registration is an establishment listing under the FD&C Act. It is not a product approval or certification of any specific product, and it is renewed annually.
Requirements Vary by Market — We Plan for Yours
Before production we confirm which labeling and documentation requirements apply to your product and destination.
| Market | Typical Requirements | Notes |
|---|---|---|
| United States | cGMP (21 CFR 111), FDA facility registration, label compliance | Dietary supplement labeling per FDA rules |
| European Union | Food supplements directive (2002/46/EC), EFSA labeling rules | Novel foods and health claim rules apply |
| Middle East / GCC | Local supplement registration and labeling | Arabic labeling often required |
| Global / multi-market | COA, heavy-metal and microbial test reports as baseline | We prioritize requirements by launch market |
Actual compliance scope depends on your formula, dosage form and destination — confirm with our sales team before ordering. Certification status of your specific products should be verified with the issuing body.
GMP-Compliant Production
Production runs in GMP-compliant facilities with batch-level control and full traceability.
COA Every Batch
Certificate of Analysis issued with every batch — assay, identity, purity and microbiology.
Documentation Support
Test reports and compliance paperwork prepared to support your import and registration.
Ask About Your Market's Requirements
Tell us the formula and destination — we'll outline the compliance path before you commit.