What is your minimum order quantity (MOQ)?

MOQ varies by product format and packaging. For most private-label lines we offer flexible low MOQs to help you test the market.

Can you develop a custom formula for my brand?

Yes. Our R&D lab creates custom formulations from your brief, with physical samples typically ready within 7–14 days.

Which certifications do you hold?

Our facility is GMP-certified and operates under ISO 9001 / ISO 22000 and HACCP systems. We also support Halal, FDA registration and SGS verification.

Do you provide packaging and labeling?

We offer full customization of bottles, pouches, boxes and labels with your brand artwork, plus barcode and regulatory labeling support.

How long does production and shipping take?

After sample approval, standard production runs typically take 2–4 weeks, followed by sea or air freight.

Which countries do you export to?

We export to 60+ countries across North America, Europe, the Middle East, Southeast Asia and Oceania.

What is the minimum order quantity (MOQ) for OEM/ODM orders?

Our standard MOQ is 3,000–5,000 units per SKU depending on the dosage form. Lower quantities may be available for market testing with a small-lot surcharge. Contact our team with your target formula for an exact quote.

Can you produce to our proprietary formula?

Yes. We accept customer-supplied formulas and can also co-develop formulas with our R&D team. A signed confidentiality agreement protects your IP throughout the process.

Health Product OEM/ODM Manufacturer | Guangzhou Kangmeihui Biotechnology

1What Is a COA?

Third-Party Testing & COA: Why They Matter · 信息卡

CategoryOEM

TagsOEM · ODM · supplements · manufacturing

PublishedAug 19, 2026

Views97 times

A Certificate of Analysis (COA) is a document issued by a quality laboratory that confirms a product meets its specifications for identity, potency, purity and safety. Reputable OEM/ODM manufacturers provide a COA for every batch.

2Why Independent Testing Matters

Third-party testing removes any conflict of interest. An accredited lab verifies that active ingredients match the label claim and that heavy metals, microbes and contaminants stay within safe limits.

3What to Check

Look for identity testing, assay/potency, microbial limits, heavy metals (lead, cadmium, mercury, arsenic), and pesticide residues. Keep COAs on file for export compliance and retailer audits.

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