United Diagnostics Analytical
Laboratory

Independent analytical laboratory

Test the material. Then make the claim.

United Diagnostics runs identity, purity, net content, elemental impurity, sterility and endotoxin analysis on research-use materials, and issues a certificate that anyone holding the vial can verify against this laboratory.

RP-HPLC-UVLC-MS/MS ICP-MSKinetic chromogenic LAL Sterility by PCR
Working laboratory bench: a stacked liquid chromatography system
                  beside a monitor running the chromatography data system, with a
                  sample table and plate map on screen.
Primary assay platform
Gradient reversed-phase HPLC with diode-array detection
11
Analytes on every
full certificate
79
Certificates issued
and verifiable
5–8 days
Typical turnaround,
full panel
QR
Every certificate
independently checkable

What a full certificate covers

Eleven analytes, each against a stated specification.

A result is only meaningful next to the limit it was judged against and the method that produced it. Every certificate we issue prints all three.

AnalyteMethodSpecification
Peptide PurityHPLC-UV, gradient RP≥ 95.0% (area %)
Net Peptide ContentHPLC-UV vs. reference standardNot less than label claim
IdentityHPLC retention timeMatches reference standard
Arsenic (As)ICP-MSNMT 1.5 ppm
Cadmium (Cd)ICP-MSNMT 0.5 ppm
Lead (Pb)ICP-MSNMT 1 ppm
Mercury (Hg)ICP-MSNMT 1.5 ppm
Chromium (Cr)ICP-MSNMT 10 ppm
SterilityNucleic-acid amplification (PCR)No growth detected
EndotoxinKinetic chromogenic LAL< 0.25 EU/mL
Fentanyl Presence AnalysisLC-MS/MS, targetedNot detected
Net content is reported as an absolute mass, not a percentage. Purity tells you how clean the material is. Net peptide content tells you how much of it is actually in the vial. A vial can be 99% pure and still be substantially underfilled. So we report both, and the content specification is not less than label claim.

Testing panels

Pick the panel that fits the material.

Every panel is quoted per submission. Email us what you have and which panel you want; we reply with price, turnaround and a submission reference to ship against.

Panel 01

GLP-1 & Incretin Analogues

Quantitative identity, purity and net content for the incretin class, including GLP-1, dual and triple agonists, and amylin analogues.

Included
  • Peptide purity by RP-HPLC-UV
  • Net peptide content per vial against reference standard
  • Identity confirmation by retention time
  • Molecular formula and CAS verification on the certificate
Turnaround
3–5 business days
Sample needed
1 sealed vial, as supplied
Request this panel
Panel 02

Research Peptides

The general peptide panel. Covers secretagogues, repair and mitochondrial peptides, melanocortins, bioregulators and blends.

Included
  • Peptide purity by RP-HPLC-UV
  • Net peptide content per vial
  • Identity confirmation by retention time
  • Per-component quantitation on multi-peptide blends
Turnaround
3–5 business days
Sample needed
1 sealed vial, as supplied
Request this panel
Panel 03

Research Chemicals & Small Molecules

Identity and assay for non-peptide research materials: small-molecule actives, oral compounds and powders.

Included
  • Assay / purity by HPLC-UV
  • Identity confirmation by LC-MS
  • Content per unit or per mL
  • Adulterant screen on request
Turnaround
4–6 business days
Sample needed
25 mg powder, or 1 sealed unit
Request this panel
Panel 04

Anabolics: Oils & Orals

Ester identification and quantitation for oil-based injectables, plus content uniformity for oral solid dosage forms.

Included
  • Ester identity and quantitation by HPLC
  • Concentration in mg/mL, oil-based preparations
  • Content per tablet or capsule
  • Screen for undeclared additional actives
Turnaround
4–6 business days
Sample needed
1 mL of oil, or 5 units
Request this panel
Panel 05

Sterility & Bacterial Endotoxin

Microbiological release testing for anything intended to be handled as a sterile preparation.

Included
  • Sterility by nucleic-acid amplification (PCR)
  • Growth-based confirmation
  • Endotoxin by kinetic chromogenic LAL
  • Result in EU/mL against a stated limit
Turnaround
5–7 business days
Sample needed
2 sealed vials, unopened
Request this panel
Panel 06

Elemental Impurities

Heavy-metal screen by ICP-MS, with limits aligned to the compendial expectations for parenteral routes.

Included
  • Arsenic, cadmium, lead, mercury, chromium
  • Limits aligned to USP <232> / <233>
  • Reported in ppm with the method limit shown
  • Extended element list on request
Turnaround
4–6 business days
Sample needed
1 sealed vial, or 25 mg powder
Request this panel
Panel 07

Adulterant & Fentanyl Screen

Targeted presence analysis for fentanyl and common analogues, run as an incoming-material integrity check.

Included
  • Targeted LC-MS/MS screen
  • Fentanyl and common analogues
  • Reported as detected / not detected
  • Extended adulterant list on request
Turnaround
2–4 business days
Sample needed
1 sealed vial, or 10 mg powder
Request this panel
Most requested
Panel 08

Full Certificate Panel

Everything above, run as one submission and issued as a single certificate of analysis with a scannable verification code.

Included
  • All 11 analytes on one certificate
  • Purity, net content and identity
  • Full elemental, sterility and endotoxin work-up
  • QR-verified certificate hosted on this site
Turnaround
5–8 business days
Sample needed
2 sealed vials, unopened
Request this panel

Methods & instrumentation

Chromatography for the assay. Mass spectrometry for the proof.

Purity as area percent comes off reversed-phase HPLC. Confirmation that the peak is the compound you ordered comes off the mass spectrometer. Elemental impurities come off ICP-MS after digestion. We do not substitute one for another.

Abstract illustration of a chromatogram: a blue trace across a dark
                    field, flat baseline broken by several sharp peaks.
RP-HPLC-UV

Reversed-phase chromatography

Gradient separation with diode-array detection. The workhorse for purity as area percent and for net content against a reference standard.

LC-MS / MS-MS

Liquid chromatography – mass spectrometry

Mass confirmation of the intended species and targeted detection of adulterants down to trace level.

ICP-MS

Inductively coupled plasma mass spectrometry

Elemental impurity quantitation in parts per million after acid digestion of the sample as supplied.

Kinetic chromogenic LAL

Bacterial endotoxin test

Endotoxin quantitation in EU/mL, read kinetically against a standard curve with positive product controls.

Nucleic-acid amplification

Sterility by PCR

Broad-range bacterial and fungal detection, paired with a growth-based confirmation before a result is released.

Reference standards

Traceable comparators

Characterised comparators for every compound we report on. Identity and content claims are made against them, never against each other.

Submitting a sample

Four steps, and a reference number the whole way through.

1

Ask for a quote

Email us the compound, the labeled content, how many lots, and which panel you want. We reply with price, turnaround and a submission reference.

2

Ship the sample

Send sealed units, unopened, with the submission reference on the outside. We log them in against the reference on arrival.

3

Analysis

Samples run inside the stated turnaround. If anything falls outside specification we contact you before the certificate is issued.

4

Certificate issued

You receive a certificate of analysis carrying a certificate number, an access code and a QR code that resolves to a record hosted here.

Abstract illustration of a microplate: an even grid of small circles,
                    a scattered few filled in blue and black among empty outlines.

Certificate verification

A certificate nobody can print at home.

Every document we issue carries a certificate number, a private access code and a QR code. The QR code resolves to a record hosted on this domain that restates the results independently of the paper. If the two disagree, trust this site.

Look up a certificate

Both values are printed on the document. The access code is the 8-character code in the reference block.

Request testing

Send us the compound and the label claim.

Tell us what the material is, what the vial says it contains, and how many lots you need covered. We come back with a price, a turnaround and a submission reference. Testing is arranged by email. There is no account to open.

Testing requests
contact@uniteddiagnostics.org
Compose a request