Accredited Peptide Testing Laboratory

The Gold Standard
in Peptide Verification.

Independent, third-party purity and identity testing for researchers, manufacturers, and the public. Every result permanently verifiable.

ISO Method Compliance
HPLC + Mass Spec
Results Never Altered
48–72hr Turnaround
Publicly Verifiable
Testing Methods:HPLC-UVLC-MS/MSICP-MSGC-FIDUSP <621>USP <731>LAL EndotoxinUSP <61/62>

Testing methods in compliance with USP, ICH, and FDA analytical guidelines

COA Verification

Public Verification.
Zero Doubt.

Every COA we issue is permanently logged and publicly verifiable. Anyone — buyer, regulator, or researcher — can confirm authenticity in seconds. No account. No fee. No waiting. We don't just issue certificates — we make them impossible to fake.

  • Immutable result records — never edited after issue date
  • QR code on every physical COA links directly to this database
  • Full testing methodology visible on every public record
  • Chain of custody fully documented from receipt to certificate
  • No account needed — public search is always free

Certificate Number

LIVE SEARCH

Live
CompoundBPC-157
Lot NumberLOT-260512-03
Purity99.2% ✓
IdentityConfirmed ✓
MethodsHPLC-UV · LC-MS/MS
Test DateMay 12, 2026

Enter any COA number to verify:

Testing Services

Complete Analytical Testing Panel

From basic purity to comprehensive safety screening — every test a serious peptide researcher or supplier needs, all under one roof.

HPLC Purity Analysis

Quantify compound purity from 85% to 99.9%+ using reverse-phase HPLC with UV detection. The industry benchmark for peptide purity measurement.

HPLC-UV · USP <621>

Mass Spec Identity

LC-MS/MS confirms the exact molecular identity of your compound — eliminating wrong-compound substitution fraud at the molecular level.

LC-MS/MS · ESI+/-

Heavy Metal Screening

ICP-MS detects lead, arsenic, mercury, and cadmium at ppb levels. Required for responsible sourcing verification and safety documentation.

ICP-MS · USP <232>

Microbial & Endotoxin

USP-compliant microbial limits testing and LAL endotoxin assay. Critical for injectable research compounds requiring sterility documentation.

USP <61/62> · LAL

Residual Solvents

GC headspace analysis per ICH Q3C for acetonitrile, TFA, DMF, and 50+ solvent residues commonly used in peptide synthesis workflows.

GC-FID · ICH Q3C

Custom Panels

Multi-compound panels, stability testing, and client-specific method development. Contact us for bespoke testing programs and volume pricing.

Custom · Contact Us
Process

From Sample to Certificate in 4 Steps

Simple, transparent, and fast. Standard turnaround is 48–72 business hours after sample receipt at our laboratory.

01

Order

Select your testing panel, complete the online submission form, and receive your unique sample ID with prepaid shipping instructions.

~5 min online
02

Ship

Package using our guidelines and ship to our lab. We accept lyophilized powder, liquid, and tablet/capsule forms. Minimum 5mg peptide.

Prepaid label included
03

Analyze

Our lab runs your sample through the ordered panel using validated, documented methods with traceable reference standards.

48–72 business hours
04

Certify

Your COA is issued via email with a unique certificate number and QR code. Results are simultaneously published to our public verification database.

PDF + public record
Why Aegis

Independence Is Not Optional

When you need to know what's actually in a compound, the only answer that matters comes from a lab with no stake in the result.

Complete Independence

We test for anyone. We work for no one. No affiliation with any peptide supplier or manufacturer. Our only interest is an accurate result — full stop.

Permanent, Unalterable Records

All COAs are write-once records. We cannot retroactively change a result — and we publish that guarantee in our terms of service for full accountability.

Full Methodology Transparency

We publish exactly how we test. Full SOPs, instrument calibration logs, and reference standards are documented on every COA. No black boxes, ever.

Speed Without Compromise

Standard 48–72 hour turnaround. Rush 24-hour service available. Real-time status tracking via client portal. No waiting in the dark for your results.

Analytical Methods

Laboratory-Grade Instrumentation

Every method is validated, documented, and traceable to international reference standards. No shortcuts, no estimations.

High-performance liquid chromatography with UV detection is the gold standard for quantifying peptide purity. Detects and quantifies impurities at the 0.05% level using validated reverse-phase gradient methods.

InstrumentShimadzu Prominence HPLC System
ColumnPhenomenex Kinetex C18, 150×4.6mm, 5µm
DetectionUV 220nm primary / 254nm secondary
Mobile PhaseAcetonitrile / 0.1% TFA in water, gradient
Flow Rate1.0 mL/min isocratic / gradient
LOQ0.05% relative purity
Reference StdUSP certified reference materials
Run Time15–25 minutes per sample
Method RefUSP <621> / ICH Q2(R1)
12,000+

COAs Issued

99.7%

Report Accuracy

48hrs

Avg Turnaround

0

Contested Results

Example Report

What a COA Looks Like

Every certificate is permanently timestamped and publicly verifiable. Here's a sample of what our clients and their buyers receive.

Aegis Peptide Analytics

Certificate of Analysis

Certificate Valid

Certificate Number

APA-2026-004821

CompoundBPC-157
Lot NumberLOT-260512-03
Purity99.2% ✓
IdentityConfirmed ✓
MethodsHPLC-UV · LC-MS/MS
Test DateMay 12, 2026
Issued2026-05-14
View Live COA →
Pricing

Transparent Testing Panels

No hidden fees. No surprise upcharges. Pick the panel that fits your needs — every test includes a publicly-verifiable COA.

Essential

$149

5–7 business days

  • HPLC-UV Purity Analysis
  • Purity % with chromatogram
  • Digital COA (PDF)
  • Public verification record
  • QR code on certificate
Order Essential
Most Popular

Standard

$275

48–72 business hours

  • HPLC-UV Purity Analysis
  • LC-MS/MS Identity Confirmation
  • Heavy metals (8 elements)
  • Digital COA (PDF)
  • Public verification record
  • Client portal access
Order Standard

Professional

$449

24–48 hours · Rush priority

  • Full Standard panel
  • Residual solvents (GC-FID)
  • Endotoxin (LAL, USP <85>)
  • Microbial limits (USP <61/62>)
  • Rush priority processing
  • Dedicated lab contact
Order Professional
Complete Panel

Comprehensive

$699

Same-day rush available

  • Full Professional panel
  • Full elemental panel (15+ elements)
  • Sterility testing (USP <71>)
  • Particulate matter (USP <788>)
  • Water content (Karl Fischer)
  • Dedicated lab scientist
  • Same-day rush option
  • Chain of custody docs
Order Comprehensive
Submit a Sample

Ready to Verify Your Compound?

Every legitimate supplier should be testing independently. Every informed buyer should be demanding it. The standard exists — we enforce it.

FAQ

Frequently Asked Questions

Everything you need to know about our testing process, results, and how to get started with a submission.

Every COA includes the compound name, lot number, purity percentage, identity confirmation, testing methods used, reference standards, instrument information, test date, issue date, and a unique COA number with QR code. Raw chromatogram and mass spectrum data is included in the full PDF report.

Once you place an order, you'll receive a unique sample submission ID and detailed packaging instructions. Ship your sample to our lab address via any carrier. Minimum quantities: lyophilized powder (5mg), liquid in sealed vials, or tablets/capsules (5 unit minimum). We provide guidance for hazardous materials shipping when applicable.

The minimum sample size is 5mg for lyophilized peptide powder. For liquids, we require at least 1mL at a concentration sufficient for analysis. Contact us for custom requirements if you have limited sample availability — we may be able to accommodate smaller quantities.

All client information is kept strictly confidential. Results are published publicly by default (linked to your COA number only), but clients may request a private COA when ordering. Private records still verify as valid — they simply don't display test data publicly. Client identity is never disclosed.

Enter the COA number printed on the document into our public verification portal at /verify. No account is needed. The portal will display the original test result as recorded at time of issuance. If the number returns no result, the document was not issued by our laboratory.

No. We have zero financial relationships with any peptide manufacturer, supplier, broker, or retailer. Our only revenue comes from testing fees paid by whoever submits samples. This independence is the foundation of our value. Our full conflict-of-interest policy is published in our Terms of Service.

A failed result is reported exactly as the data shows — FAIL status with the actual measured values. We do not offer re-testing opportunities that could influence results. Clients receive the full PDF report regardless of pass/fail outcome. We recommend contacting your supplier with the result documentation.

We test any synthetic peptide including research peptides (BPC-157, TB-500, GHK-Cu, Epithalon), GLP-1 analogs (Semaglutide, Tirzepatide, Retatrutide), growth hormone peptides (Ipamorelin, CJC-1295, GHRP-6), and custom sequences. Contact us for unusual compounds to confirm feasibility before ordering.