Factory & quality documentation
Quality you can review, document by document.
Confirm the production route, facility and applicable evidence for your product before approving an order.
Manufacturing site
Request the legal entity, actual production location and product scope for the quoted project.
Applicable certificates
Check the issuing body, site address, validity period and whether the stated scope covers your product route.
Finished-product evidence
Agree the relevant test methods, acceptance criteria and batch documents for the actual formula.
Documents to request during supplier review
| Document | What to verify |
|---|---|
| Facility and certificate information | Current issuer, address, validity and product/process scope. GMP, ISO or HACCP references are questions for review, not certification claims for this website. |
| Ingredient specification | Identity, source, relevant active content, carriers and lot traceability. |
| Certificate of analysis (COA) | Sample identity, lot number, test methods, limits, results and release responsibility. |
| SDS where applicable | Material identity, handling information and version. An SDS is not proof of efficacy or market approval. |
| Finished-product specification | Fill weight, pouch format, analytical scope, relevant microbiology and packaging checks. |
| Stability and storage record | Actual formula, packaging system, study conditions and support for the proposed shelf life. |
Why no certificate gallery or factory photo claims?
Certificates and facility photographs must be current, relevant and tied to the actual manufacturing arrangement. Until approved documents and verified photographs are provided for publication, this site uses clearly identified workflow illustrations. Request the project-specific document package directly from our team.
An approval checklist for your SKU
- Ingredient and supplier identity reviewed.
- Agreed analytical and microbiological test scope documented.
- Formula, sample, can, artwork and carton versions matched.
- Destination-specific ingredient and label questions resolved by responsible parties.
- Release responsibilities and deviation handling agreed.
Request the documents relevant to your project.
Share your destination, ingredient direction and quantity per SKU. We will review the details before confirming feasibility, cost or timing.
EMAIL: info@linkbiolabs.com
WhatsApp: +86 139 8303 6513
From material handling to the production line. Company-supplied footage showing material handling, equipment and controlled production areas. Discuss the proposed facility, line configuration and document scope alongside your formula and packaging brief. Review the company-supplied document overview, then request the current documents relevant to your project. Open the overview to inspect the supplied image. Certificate holder, validity, certified site and product scope are checked against the current documents for each project. Choose your flavors, can format and artwork around one production brief.A closer look at manufacturing.
Manufacturing overview
Connect the footage to your project.
Discuss production requirementsQualification documents, ready for review.
A clear starting quantity.