Every batch PeptideVault ships is synthesized in the United States, independently lab-tested before release, and tracked from compounding to your door. Here is exactly how that works — and the paperwork that proves it.
Synthesis takes place in American cGMP facilities. No overseas brokers, no relabeled imports — every amino-acid chain starts inside a US-based compounding lab.
Peptides are dispensed patient-specifically through licensed Section 503A compounding pharmacies, under a physician-signed prescription, every time.
A licensed physician signs off on every prescription. The protocol is matched to your goals and labs — not a templated supply order.
The amino-acid sequence is assembled in a US cGMP lab under controlled conditions, with full lot tracking from raw materials onward.
A retention sample is pulled from every production batch, sealed, and sent to an independent third-party laboratory — never in-house.
The third-party lab runs high-performance liquid chromatography and mass spectrometry to verify identity, purity, and the absence of residual solvents.
Returned results are checked against release specifications — purity ≥ 98%, endotoxin < 0.25 EU/mg, identity confirmed — before the lot is cleared.
Only after the Certificate of Analysis is matched does the batch move to dispensing, cold-chain fulfillment, and tracking the unit all the way to delivery.
Redacted sample — per-batch COAs are issued with every PeptideVault order.
| Product | BPC-157 (lyophilized) |
|---|---|
| Batch ID | PV-2026-0618-04 |
| Synthesis Date | 2026-06-18 |
| Purity (HPLC) | 99.7% |
| Endotoxin (LAL) | < 0.25 EU/mg |
| Test Date | 2026-06-22 |
| Verifying Lab | NorthStar Analytical Labs (independent, third-party) |
Released under prescribed spec — see your order's COA PDF for the full panel (heavy metals, residual solvents, microbial).
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