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Are you willing to sign a Quality Agreement specifying product specifications and QC obligations?
Yes. We routinely sign Quality Agreements with international buyers, particularly in the food, beverage, and pharmaceutical industries. A Quality Agreement is a formal document that defines the product specification, testing requirements, non-conformance procedures, and mutual quality obligations — providing legal and technical clarity for both parties.
Quality Agreement Covers
| Section | Content |
|---|---|
| Product specification | Exact Mogroside V content, appearance, particle size, etc. |
| Testing requirements | Which tests, frequency, and acceptance criteria |
| Certificate of Analysis | What the COA includes and when it is issued |
| Non-conformance | Defective product handling, returns, and credit procedures |
| Change notification | If we change raw material source or process |
| Shelf life & stability | Storage conditions and guaranteed shelf life |
| Audit rights | Your right to audit or request third-party inspection |
| Confidentiality | Product specification confidentiality |
For orders above USD 20,000, a signed Quality Agreement is a standard requirement before we proceed with production. Send your standard Quality Agreement template or request our template to start the process.
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This article was published on 2026-09-02, and last updated on 2026-09-02. The article will be continuously updated.
