Independent analytical lab · EU

Purity you can verify, not just trust.

Meridian Bioanalytics runs HPLC purity quantification and mass-spectrometry identity confirmation on research peptides and other compounds. Every result resolves to a public certificate you can check yourself.

99.9%
purity resolution
48h
standard turnaround
UHPLC
+ LC–MS/MS
Meridian certificate of analysis for BPC-157 at 99.4% purity
ISO/IEC 17025 accredited methods GLP & European Pharmacopoeia Independent of every vendor 48-hour standard turnaround HPLC purity + LC–MS/MS identity Publicly verifiable certificates Endotoxin & heavy-metal panels Traceable reference standards ISO/IEC 17025 accredited methods GLP & European Pharmacopoeia Independent of every vendor 48-hour standard turnaround HPLC purity + LC–MS/MS identity Publicly verifiable certificates Endotoxin & heavy-metal panels Traceable reference standards
What we test

One bench, the full analytical picture.

From a single vial we confirm what a compound is, how pure it is, and how much of it you actually received — plus the contamination panels that separate a real lab from a self-reported claim.

HPLC purity

Reversed-phase UHPLC resolves the main component from synthesis by-products and degradation, reported as area-% with the full chromatogram.

RP-UHPLC · UV/DAD

LC–MS/MS identity

Mass-spectrometry confirms the molecule is the claimed compound by matching measured mass to the expected molecular weight.

ESI · m/z confirmation

Quantitative content

Net peptide content per vial — the actual milligrams present versus the label claim, so a 10 mg vial is verified as 10 mg.

mg/vial · net content

Endotoxin (LAL)

Bacterial endotoxin screening to USP <85> / Ph. Eur. limits — essential for material intended for sensitive in-vitro work.

EU/mg · USP <85>

Heavy metals & residuals

Elemental impurity screening and residual-solvent / water-content checks for full-panel assessment of unknown sources.

ICP-MS · ppm

Sterility & full vial

Sterility and bioburden assessment, combined into a single full-vial report alongside identity, purity and content.

bioburden · full panel
Also tested: SARMs, anabolic compounds, raw chemicals, nutraceuticals & supplement actives — same chain of custody, same public verification.
Inside the lab

A working analytical bench, not a drop-shipper.

Samples are received, logged under chain of custody, and run on the same validated instruments every time. Nothing is outsourced and nothing is estimated — every figure on a certificate comes off our own bench.

UHPLC + LC–MS/MS systems, mirrored for redundancy so maintenance never delays your result.
Traceable reference standards from recognised pharmacopoeial directorates.
Chain-of-custody logging from intake to released certificate.
Analyst operating an HPLC instrument at the Meridian bench
Public verification

Every certificate is checkable at the source.

A certificate of analysis is only worth what you can independently confirm. Each Meridian report carries a unique ID that resolves to a record on our servers — not on a vendor's website. Enter a report number to see what a buyer sees.

Try a sample report:
MB-2026-100423 · MB-2026-100876 · MB-2026-101204
How it works

Four steps from vial to verified certificate.

Row of sealed analytical sample vialsevery vial in → one verified certificate out
01

Request a quote

Tell us the compound, format and assays you need. We confirm price, sample amount and the deadline before you ship.

02

Ship your sample

Send the vial with its batch reference. We provide packaging and customs guidance for EU and international couriers.

03

Analysis on the bench

Validated UHPLC and LC–MS methods run against traceable reference standards, with redundant instrumentation to avoid delays.

04

Verified COA

You receive a batch-specific certificate with the chromatogram and a permanent public verification link & QR code.

Why Meridian

Reliability is in the details.

Deadline or it's free

A full refund and free re-analysis guarantee applies to any report not completed by the agreed deadline. No exceptions, no fine print.

Instrumentation, doubled

UHPLC and LC–MS systems are mirrored, so routine maintenance never becomes your delay. Day-to-day equipment is held to the same bar as the headline instruments.

Traceable reference standards

Standards sourced from recognised pharmacopoeial directorates and reference institutes, with chemicals carrying their own certificates of analysis.

Genuine independence

We are not owned by, affiliated with, or paid based on the result of any peptide or compound vendor. The number on the certificate is the number we measured.

Pricing

Per-assay, transparent, no bundles you don't need.

Indicative pricing for routine analyses. Final quotes are confirmed per sample based on matrix and assay combination.

AnalysisWhat it answersFrom
HPLC purityArea-% purity with full chromatogram€69
LC–MS identityConfirms the compound is what's claimed€89
Quantitative contentActual mg per vial vs. label claim€79
Endotoxin (LAL)Bacterial endotoxin to Ph. Eur. limits€95
Full vial assessmentIdentity + purity + content + sterility€229

Pricing in EUR · volume & recurring-batch rates on request · crypto and SEPA accepted.

Get started

Ready to test a batch?

Request a quote and shipping instructions. Most routine reports are completed within 48 hours of sample arrival.