Supplier audit
Review the source through on-site inspection, certification verification, capacity assessment, and production controls.
Quality & documentation
STARORAN coordinates supplier qualification, batch review, independent testing, pre-shipment checks, and applicable documentation.
Independent assurance
Before approval, every manufacturing partner undergoes supplier qualification covering on-site inspection, certification verification, and production-capacity assessment.
Our QC team coordinates independent third-party testing for every batch before shipment. The confirmed scope includes testing for purity, heavy metals, microbiological parameters, and pesticide residues where applicable.
Four quality checkpoints
Review the source through on-site inspection, certification verification, capacity assessment, and production controls.
Verify raw-material identity, condition, and product information when material is received.
Coordinate third-party laboratory testing for every batch against the confirmed test scope.
Complete final QC and review packaging, documents, and order details before shipment.
Batch-linked results and product information for the material being supplied.
Available safety, handling, storage, and transport information for the product.
Identity, physical format, assay, limits, and other agreed technical parameters.
Applicable source, test, origin, regulatory, and packaging information requested for review.
Global regulatory support
We help coordinate information relevant to FDA requirements, EU Novel Food reviews, cGMP standards, and NDI notifications. Buyers remain responsible for determining whether the ingredient, specification, claims, labeling, and document set meet the legal and technical requirements of the intended market and use.
Request available information