Aegis Peptide Analytics was founded on a single premise: the peptide research and supply industry needed a genuinely independent testing laboratory — one with no affiliations, no conflicts of interest, and no incentive to produce any result other than the true one.
Our Mission
“To provide the peptide research community with independent, scientifically rigorous testing that makes fraud difficult, accountability real, and trust possible.”
— Aegis Peptide Analytics founding charter, 2025
Every analytical laboratory faces a fundamental question: who does the data serve? At most labs, the answer is the client who paid. At Aegis, the answer is the truth.
We enforce our independence through structural means — not just policy. We do not accept equity, commissions, referral fees, or any form of compensation from any entity in the peptide supply chain. Our revenue is testing fees only.
Our conflict-of-interest policy is published publicly. Any violation by any staff member is grounds for immediate termination. This is not a soft commitment — it is the precondition for everything we do.
These are not aspirations — they are operational commitments enforced through systems, policy, and public accountability.
We test for anyone. We work for no one. Aegis has zero financial relationships with any peptide supplier, manufacturer, retailer, or broker. Our only revenue comes from testing fees. Full stop.
Every COA we issue is write-once. We have architected our systems so that results cannot be retroactively modified after certificate issuance. We publish this guarantee in our terms.
We document everything. Every COA includes the exact instrument, method, reference standard, and calibration data used. No black boxes. No proprietary secrets. Full methodology visible.
We built efficient workflows that deliver 48–72 hour turnaround without cutting analytical corners. Our clients shouldn't have to choose between speed and accuracy.
Our public verification portal exists because we believe all COA data should be verifiable by anyone — buyers, regulators, and the public — not just the entity that paid for the test.
All methods are validated against USP, ICH, and FDA analytical guidelines. We use certified reference standards, calibrated instruments, and documented procedures for every single test.
COAs Issued
Report Accuracy
Avg Turnaround
Contested Results
Whether you're a researcher verifying a single batch or a manufacturer building a compliance program, we have a panel that fits.