← Quality & Compliance Overview
Supplement Regulatory Support
Navigate global supplement regulations with expert guidance.
Your dossier, prepared before you sample
IN-HOUSE CAPABILITY
Regulatory requirements differ market by market, and a formula that is straightforward in one country can need a different label, a different claim set or a different specification in another. We review that before sampling rather than after the order is placed.
- Handled by our own team in Zhengzhou, not brokered out
- Documented at every step and released against a written specification
- Pilot-scale trial before you commit to a bulk order
Regulatory requirements are the part of a supplement project that customers most often underestimate, and the part where we are most careful about what we claim. What follows is what we actually do, and what stays with you.
What we prepare
- Ingredient review against the permitted list for your destination market
- Label wording review, including mandatory statements and claim boundaries
- Certificate of Analysis, specification sheet, nutritional panel and allergen statement
- Facility certificates and registrations required by the importing market
- Documentation packs for your own registration submission
Market snapshot
| Market | Typical focus |
|---|---|
| United States | FDA food facility registration, labelling and structure/function claim wording |
| European Union | Food supplement directives, permitted vitamins and minerals, novel food status |
| United Kingdom | Post-transition labelling and notification requirements |
| Turkey | Import registration and Turkish-language labelling |
| Middle East | HALAL certification and Arabic labelling |
| South East Asia | Varies by country — case-by-case review |
What stays with you
Product registration in your own market normally requires a local entity. We can supply the manufacturing and facility documentation that goes into your submission, but we do not register products in your name, and we are not a law firm or a regulatory consultancy — for legal opinions on claims or classification you should instruct a local specialist.
Why we state limits explicitly
A manufacturer that promises to “handle all compliance” is promising something it cannot deliver. Knowing where our side of the line sits is what makes the rest of the documentation trustworthy.
See certifications for what our facility holds today, and export documentation for the paperwork issued per shipment.
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.
HOW IT WORKS
What We Review
Ingredient permissibility, label text and claim wording, allergen and nutrition declarations, and the certificates your importer will ask for. Our documentation set covers GMP, ISO 22000, HACCP, HALAL and FDA facility registration, with batch-specific records issued per shipment.
