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From supplier to supporting evidence.

How we review supplier certificates, commission sample testing and obtain LabDoc verification.

Our Testing Process

  1. 01

    Prequalified supplier network

    Neo Labs sources compounds through its prequalified supplier network.

  2. 02

    Supplier CoA review

    Neo Labs reviews and validates supplier-issued Certificates of Analysis for each compound.

  3. 03

    Batch-matched sample testing

    Neo Labs commissions HPLC testing of selected product samples matched to their relevant batches.

    Ozcanium Analytics Retatrutide 10mg laboratory report
  4. 04

    LabDoc verification

    Neo Labs submits the relevant HPLC testing documentation to LabDoc for independent verification and assessment of result consistency.

    LabDoc verification of the Ozcanium Retatrutide 10mg report
  5. 05

    Neo Labs release review

    Neo Labs reviews available documentation before making products available to researchers.

Testing applies to the sampled batch. Neo Labs does not commission independent testing of every batch. Supplier CoAs, selected sample testing and LabDoc document verification provide different forms of evidence; coverage varies by product and batch. LabDoc reviews the submitted documentation and does not perform the original HPLC testing.

See how the evidence connects.

One example: Retatrutide 10mg · source batch 21/08/2026 · tested 24 August 2026.

01 / Original laboratory report — Ozcanium Analytics
Original Ozcanium report OZ-HPLCMS-NEO1: Retatrutide 10mg, purity 99.57%, content 10.45mg
02 / Verification of that report — LabDoc
LabDoc report LD-C367B70B7-10 reviewing the same Ozcanium report: purity 99.57%, content 10.45mg, identity confirmed

Both documents refer to the same tested sample and source report, OZ-HPLCMS-NEO1. The original analysis was performed by Ozcanium Analytics; LabDoc reviewed and published its assessment of that laboratory evidence. These reports do not establish the results for other batches.

What the results tell you

Purity

The proportion reported by the analytical method.

Measured content

The amount of compound reported in the tested sample.

Identity

Whether the reported analysis supports the compound’s identity.