Our 8-step verification protocol ensuring analytical-grade authenticity for every batch. From blind entry to public COA.
No manufacturer claims accepted. We verify first, label second.
Random vials pulled from sealed production batches for testing.
Secured shipment to Janoshik, Prague, CZ.
Quantitative analysis via high-performance liquid chromatography with diode array detection.
Molecular confirmation via liquid chromatography tandem mass spectrometry.
Bacterial contamination testing using limulus amebocyte lysate assay.
≥99% purity, confirmed molecular identity, ≤0.1 EU/mg endotoxin. No exceptions.
Full Janoshik report published. Every vial QR-scans to its chromatogram, mass spectrum, and endotoxin data.
Enter any Vantix batch ID to view the complete analytical analysis — HPLC chromatogram, mass spectrum, and endotoxin screening.
Open Verification Portal →