Quality & Verification

Six stages.
Nothing ships without them.

Every Vertalis batch passes a documented six-stage quality pipeline before it reaches your lab. No exceptions. No batch-skipping. No shortcuts.

≥99% Purity Baseline100% Third-Party VerifiedPublicly Archived COAsLyophilized · Ships Ambient
/ 01 · The Pipeline

From raw material to your bench.

01

Sourcing

All raw materials are procured exclusively from vetted synthesis partners operating under strict NDAs. Every supplier undergoes facility audit and documented chain-of-custody verification before we accept a single gram of material.

02

Synthesis

Peptides are synthesized via solid-phase peptide synthesis (SPPS) in ISO-controlled cleanroom environments. Sequence fidelity is verified at synthesis before lyophilization.

03

Internal QC

Each batch undergoes internal quality control including visual inspection, moisture content (Karl Fischer), and preliminary identity screen before being submitted for external testing.

04

Independent Testing

Every lot is independently analyzed by our third-party laboratory partners using HPLC-UV, LC-MS/MS, and LAL endotoxin assay. Results are not released internally before testing clears.

05

COA Publication

Certificates of Analysis are published publicly and indexed by batch code the moment they pass all thresholds. No batch ships before its COA is live.

06

Ambient Dispatch

Vials are sealed in inert atmosphere and dispatched via standard courier within 24h of payment confirmation. Lyophilized peptides are shelf-stable at ambient temperature, so no cold-chain packaging or ice packs are required.

/ 02 · Testing Methodology

What every COA covers.

HPLC Purity

High-performance liquid chromatography confirms purity ≥99.0%. Full chromatogram published in every COA.

LC-MS/MS Identity

Liquid chromatography–mass spectrometry confirms molecular weight and sequence identity against theoretical values.

Endotoxin (LAL)

Limulus Amebocyte Lysate assay confirms endotoxin levels below 5 EU/mg. Critical for in vitro research integrity.

Microbial Limits

Microbial contamination screening ensures sterility for research applications requiring clean environments.

/ 03 · Testing Partners

The labs behind every COA.

We work exclusively with accredited, internationally recognized analytical laboratories. All are independent. They report results to us, not the other way around.

Verify any batch in seconds.

Enter a batch code from any Vertalis vial to retrieve the full COA.

COA Archive
GLP-3 (RT) - 10MG

Jordan K. · Toronto, ON

GLP-3 (RT) - 10MG

Purchased 12 minutes ago