Product identity
Product name, material source, key composition and the claims the material does not support.
Documents & quality
We separate product identity, product specification, batch evidence and facility information so that each document is used only for the claim it can support.
Product name, material source, key composition and the claims the material does not support.
Target parameters, test methods, storage, shelf life and packing for the reviewed item.
A certificate of analysis for the relevant lot, used only within that lot's scope.
Manufacturing or quality documents stated at facility level when that is their actual scope.
Public buyer resources
These public PDFs summarize the current reference profile and the information needed for a useful first review. Batch COAs, MSDS files and facility documents remain project-specific.
Identity boundary, typical assay, reference packing, shelf life and buyer review checklist.
Open product sheet →Hydrolyzed identity boundary, molecular weight, protein, packing and buyer review checklist.
Open product sheet →Claim boundaries
A facility-level NSF GMP registration is described at facility level. It is not presented as an NSF-certified ingredient.
We do not call an ingredient “FDA approved” or “TGA approved” without an applicable, product-specific basis.
Reference COA values describe the stated lot. Commercial supply follows the document set for the lot being offered.
Before requesting documents
Start with the facts
Share your target specification, application and estimated quantity. We will reply with the right document and sample path.