Independent Analytical Laboratory

Identity and purity,precisely determined.

Verum Analytical is the analytical layer between makers and the people who rely on accurate labels. We analyse peptides and research compounds against documented methods, and issue a Certificate of Analysis for every batch — each one verifiable at source.

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Certificates Issued
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On-Time Delivery
0–7d
Standard Turnaround
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Records Retained
Services

One laboratory, the full release panel.

Each determination is tied to a documented method and a qualified instrument, and can be commissioned on its own or combined into a batch-release package.

01

Identity

Confirms the compound matches its declared structure and mass, and separates it from close analogues.

LC-MSHRMS
02

Purity & Related Substances

Resolves the main component from impurities and degradants, each reported by area percent.

RP-HPLCUHPLC
03

Quantitative Assay

Determines how much labelled compound is present, against a traceable reference standard.

HPLC-UV
04

Water & Residual Solvents

Residual water, counter-ion and process solvents that shift mass balance and true content.

Karl FischerGC
05

Elemental Impurities

Trace catalytic residues and heavy metals, reported element by element to ppb.

ICP-MS
06

Endotoxin & Sterility

Bacterial endotoxin and recoverable microbial growth for material presented in injectable format.

LALUSP <71>
Accepting New Partners

Scientific precision at commercial speed.

A foundation for companies that value efficiency, quality and integrity as they scale.

Quick turnaround
Results faster than any other lab in the region — 5–7 days standard, with a 1-day rush option.
PhD-verified accuracy
Every certificate reviewed by qualified professionals before release.
Trusted by 300+ clients globally
Batch VER-2026-0892
GHK-Cu · Full Release Panel
Purity by RP-HPLC99.70% PASS
Independent by Design

We analyse. We don't make or sell.

Verum Analytical has no stake in what it measures. Every result is reported within a defined scope of testing — a statement of exactly what was determined and how — with each figure traceable to its method.

Documented, validated methods
Every test follows a written SOP with traceable instrument calibration.
Orthogonal confirmation
Key findings are cross-checked with independent techniques before release.
Traceable reference standards
All quantitative work is anchored to certified reference materials with known purity.
Independent review before release
No certificate leaves the lab without secondary review by a separate qualified analyst.
Records retained seven years
Complete analytical records, chromatograms, and raw data archived for regulatory audit.

Precision instruments.
Impeccable records.

From Agilent and Waters HPLC systems to PerkinElmer ICP-MS, every instrument is qualified, maintained, and traceable to NIST-recognised standards.

How It Works

From sample to certificate.

A clear, traceable path from your material arriving at the bench to a verifiable Certificate of Analysis in your hands.

01

Request

Tell us the compound and the determinations you need. We confirm methods, scope and turnaround before any work begins.

02

Scope & Quote

We confirm methods, scope and turnaround before any work begins. No surprises, no hidden fees.

03

Ship the Sample

Send the material by prior arrangement, labelled with your reference. Chain of custody begins on receipt.

04

Analysis

The sample runs its method panel on qualified instruments. Raw data is reviewed and calculations verified.

05

Certificate

A documented COA is issued, verifiable at source by QR or lot number. Immutable once finalized.

Have a batch that needs analysis?

Tell us the compound and the determinations you need. We'll confirm scope, turnaround and how to ship the sample.