Methodology

How We Test

Our plan for lot testing and publication.

For each lot intended for sale, Purity Forge plans to submit a sample to an analytical laboratory and publish the original lot-specific report before release.

01

Lot identification

Each lot approved for release will receive a unique identifier. The same identifier will appear on the released vial and its public record.

02

Analytical scope

Each record will list the analyses, methods and results in the original laboratory report. Purity, identity and quantity results will appear only when those tests were performed and reported.

03

Public lot record

Each released lot will have an entry in the public COA library, linking the material and lot identifier to the issuing laboratory, reported methods and results, and original source file.

04

Verify the record

Match the lot identifier and labeled quantity on the vial to the public record. Then confirm the material, laboratory, reported methods, and source document.

All Purity Forge Labs products are labeled strictly for laboratory Research Use Only — not for diagnostic, therapeutic, or any clinical use in humans or animals.

This is the planned prelaunch standard. No live lot results are shown on this page.

Preview the COA formatBrowse research catalog