Testing process

Five steps. Two labs.
One batch number.

01 / 05

Synthesis

Solid-phase peptide synthesis at a cGMP-certified partner facility. Every reaction batch is logged with full traceability to raw material lot.

02 / 05

First-pass analysis

Internal HPLC-UV and LC-MS confirmation. If purity is below 98.5% the batch is discarded — not re-purified, not blended, discarded.

03 / 05

Third-party verification

A representative sample is shipped to an independent lab (Janoshik Analytical or Auxilium Pharma Labs) for blind verification.

04 / 05

Lyophilization & QC

Approved batches are lyophilized, sealed under inert gas, and stored at −20°C until dispatch.

05 / 05

Cold-chain dispatch

Vacuum-insulated container sized to weight and destination zone. Temperature data logger included on shipments over $400.

Certificate of Analysis
Janoshik Analytical
Independent Third-Party Lab · Slovakia
Batch
B-2026-014
Compound
BPC-157
Test Date
22 Jan 2026
CAS Number
137525-51-0
Method
HPLC-UV / LC-MS
Purity Result
99.4%
single peak · 220 nm
Contaminants Panel
  • Endotoxins < 0.5 EU/mg
  • Heavy metals Not detected
  • Residual solvents Below LOQ
  • Bioburden < 10 CFU/g