Report-reading checklist

A COA is not one thing.

Identity, purity, content, sterility, and endotoxin are different questions. Check what the report actually measured before repeating its conclusion.

Record context

Can this report be connected to this item?

Measurements

Which question did each test answer?

FieldWhat it can supportWhat it does not establish alone
Mass spectrometry / identityEvidence consistent with a stated molecular identity under the method used.Net content, sterility, or clinical effect.
HPLC purityRelative purity under the reported chromatographic method.Identity, total amount, sterility, or absence of every contaminant.
Net content / assayMeasured amount under the reported quantitative method.Sterility, identity unless coupled with an identity method, or future-batch consistency.
SterilityResult under the stated sterility method and conditions.Endotoxin absence, identity, or every possible contaminant.
EndotoxinEndotoxin result against the stated method/limit.Sterility, purity, or clinical suitability.
Heavy metalsReported metals under the stated panel and detection limits.Other contaminants, sterility, identity, or content.
Stronger context

Traceable and relevant

Named lab, verifiable report ID, matching batch, documented sample path, and methods that answer the claims being made.

Incomplete

Important gaps

A real-looking report can still be disconnected from the unit, batch, seller, or claimed measurement.

Seller claim only

Not independently checked

Marketing copy, cropped screenshots, copied PDFs, and unverifiable certificates remain seller claims.