Every compound in the P3X Labs catalog moves through a documented four-step chain of custody before it reaches the vial label.
1. Synthesis
Compounds are sourced from manufacturers audited for Good Manufacturing Practice (GMP) compliance. Sourcing partners undergo routine review; contracts require per-batch certificates of analysis issued by the synthesis lab.
2. Import & custody
Batches are imported into the United States and delivered into the custody of a third-party logistics provider. Chain-of-custody records are maintained from port of entry through the 3PL receiving dock.
3. Independent testing
Every batch is tested by Freedom Diagnostics Testing (FDT), an independent accredited laboratory. FDT issues a per-batch Certificate of Analysis (COA) covering identity, purity, and endotoxin levels. Batches that do not pass FDT release criteria never enter the catalog.
4. Labeling
Each vial label carries a QR code that links to the FDT COA for that specific batch. The labeled vial is sealed, and the 3PL maintains custody until shipment. Scan the QR on any vial to pull up the COA — no account required.
What this is not
P3X Labs products are research compounds, not a drug, dietary supplement, or medical device. They are sold exclusively to qualified research professionals. See our testing methodology for details on the FDT testing scope and COA format.