Every batch of every P3X Labs compound is independently tested by Freedom Diagnostics Testing (FDT) before it is labeled and shipped. FDT operates an accredited laboratory; their testing methodology is the basis for our Certificates of Analysis (COA).
What FDT measures
- Identity — the compound matches its declared structure (by HPLC and MS)
- Purity — reported as a percentage of the total peak area by HPLC
- Endotoxin — LAL assay, reported in EU/mg
- Net fill / mass — confirmed against declared vial content
Batch-level traceability
Every vial label carries a lot number in the canonical format FDT-YYYY-NNNNNN alongside a QR code. Scan the QR to open a batch-specific COA. The same lot number appears on our internal records and the 3PL manifest — end-to-end traceability from the independent lab to the shipping label.
What the COA shows
The COA is a one-page document on FDT letterhead, signed by the laboratory director. It includes the batch identifier, the methodology used for each measurement, the results, and a release determination. Batches that do not meet release criteria do not enter the catalog.
At fulfillment, each vial carries a scannable QR that opens the batch COA.
What this page is not
This page describes the testing methodology we use to release batches. P3X Labs products are research compounds — sold for research purposes only, not for human or veterinary consumption. See our supply chain page for the full chain of custody.