Quality & testing

Frequently asked questions

What documents are included with VaultLabs materials?

Each catalogue batch is tested twice before release. Each order ships with a Certificate of Analysis and a traceable lot number. Identity and purity appear on the COA — match your vial label to the record on batch verification. Document type is labelled on each record.

What purity levels are documented?

Published COA records report purity for the specific lot tested — often above 99% when that figure appears on the certificate. The exact purity value is batch-specific on the certificate.

What is the difference between identity and purity?

Identity confirms the material matches the expected compound. Purity describes the proportion of the target compound relative to detected impurities in the analytical method used. They answer different laboratory questions.

Does purity equal the labelled amount in the vial?

No. Purity is an analytical ratio. Labelled quantity (for example 10 mg) is a separate specification that may be supported by quantitative testing when published for that lot.

Is each batch tested more than once?

Yes. Each catalogue batch is tested twice before release — a first assay and a confirmation assay. Partner laboratories include Janoshik Analytical, METS Lab, and Freedom Diagnostics. The laboratory printed on the published certificate is the laboratory for that lot, and a batch shows Janoshik, METS, or Freedom only when that lot has their report.

What is the difference between supplier and independent testing?

Supplier or internal documents reflect release and handling records from the supply chain. Independent third-party testing is performed by an external laboratory. VaultLabs labels document type clearly on verification results — a PDF alone is not automatically independent testing.

What does pending or unavailable mean?

Pending means the record exists in workflow but is not yet published online. Unavailable means no document is currently published for that lot and test type. Neither status implies a pass or fail result.

Who tested the current GLP-3 RT 10mg lot available in the UAE?

The current published GLP-3 RT 10mg (Retatrutide) shipping lot in the UAE is 20280309. The laboratory named on that certificate is Freedom Diagnostics. Published purity is 99.94% by HPLC-UV / LC-MS, search code Vaul2609221080. VaultLabs dispatches this line from Dubai to all seven emirates with checkout in AED. Janoshik Analytical and METS Lab are named counterparties; they appear on a batch only when that lot has their report. This lot’s published report is Freedom Diagnostics only.

How do I verify a report?

Use the lot number on your vial label in the batch verification portal. The published COA and test record should match your catalogue number, lot, and document type — this confirms you are viewing the correct certificate for your material.

What does VaultLabs not claim?

VaultLabs does not claim medical, therapeutic, or personal-use suitability. Published analytical records describe material characteristics for research use — not clinical outcomes or sterility for human use. A partner laboratory name is not a substitute for the laboratory printed on that lot’s certificate.