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Batch-document guide

Read the record. Match the material.

A certificate of analysis describes the sample and findings identified in that report. Match the supplied material to the original document before relying on its results.

What is a certificate of analysis?

A certificate of analysis, or COA, records stated analytical findings for an identified sample or batch. Its useful evidence is the report’s actual identity, methods and results. A general compound description, product photo or published paper is separate from a COA for a supplied vial.

Start with the label and SKU

Horizon lists a distinct SKU for each vial size. For example, BPC-157 10mg is HM-BPC-157-10. The 10mg label is a material quantity, not a dose, and the SKU identifies the catalog selection. Neither is a laboratory result or a substitute for a supplier lot record.

A practical document checklist

  1. Compound: Does the named material match the vial and supplier specification? Note any salt form, modification or blend detail stated in those records.
  2. Lot or sample identity: Does the report identify the batch or sample linked to the supplied material? Ask for the connection if the identifiers differ.
  3. Quantity and formulation: Check the labeled size where applicable. A blend’s total fill does not establish its ingredients or individual quantities.
  4. Report issuer and date: Identify who issued the report and when the reported testing occurred. Do not infer laboratory accreditation from a logo or a listing.
  5. Methods and findings: Read the stated tests, units and results, along with any specifications or limitations. Do not extend one result to a property the report does not address.
  6. Original document: Read the published source PDF rather than relying on a badge or summary. If information is missing or inconsistent, ask before relying on it.

What a result does not establish

A reported purity figure is a finding within that report’s methods and scope. It is not an administration instruction, proof of sterility, a clinical benefit claim or permission for human or animal use. A paper about a named peptide is not evidence that a Horizon batch was tested.

What “COA pending” means at Horizon

A pending label means no original report is currently published for that selection. No purity, sterility, accreditation or passing-result claim is substituted for missing evidence.

How to resolve a mismatch

Compare the compound, selected size and available lot identifier. Send those details to support@horizonmolecular.com, explaining which document field is missing or different. Avoid sending medical information or payment details.

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Materials are exclusively for laboratory research, not for human or animal use. This checklist helps interpret documents; it does not certify any vial or assess a laboratory protocol.