Eighteen categories. HPLC, MS, ICP-MS, GC-MS, endotoxin, sterility, pH and more offered across categories.
Identity, purity and net peptide content for GLP-1 class, blends and injectable safety panels.
Potency, identity and analog screen for capsules, liquids and powders, with label claim verified.
Mitragynine and 7-OH quantification, heavy metals, microbial limits and pesticide residue.
Label-claim verification, vitamin and mineral potency, heavy metals and undeclared ingredients.
Active potency, preservative efficacy, heavy metals and microbial limits for serums, creams and topicals.
TPH by carbon range, BTEX and the 16 EPA priority PAHs in soil, water, fuels and used oil.
Multi-residue panel plus glyphosate and AMPA in produce, botanicals, soil and water samples.
PFAS, metals under the Lead and Copper Rule, Closer to Zero panels and mycotoxins.
Lower fees, and listings built to be found by labs searching for equipment. Buy used equipment, sell or trade in yours, or consign it with us. Every lot is photographed as it ships and says what has not been verified.
Most laboratories ask you to trust the certificate. We publish the evidence behind it. From the carrier scan to the signed certificate, every stage of your sample's handling is recorded, tied to its accession number, and available to you: the unboxing video, a photograph of each container, the calibration status of the instrument it ran on, the raw data files, and the analyst who signed. No other laboratory publishes this record.
Your carrier tracking number is matched to your order at the desk. The sealed package is weighed and photographed before anyone opens it, so the record starts before we touch the contents.
This is an illustrative, AI-generated workflow film. It is not a recording of a specific accession and is not a chain-of-custody record.
Three safeguards keep each certificate tied to the sample we tested and the client we issued it to.
Filmed receipt, container photos and blind codes connect the tested sample to its accession and analytical record.
Every package is opened on camera, each container is photographed and blind-coded before the bench sees it, and the footage, photos, instrument ID and raw data are linked to the accession. Anyone holding the certificate can trace it back to the vial that was tested. No other laboratory publishes that chain.
Client branding, the lot, a document hash and a verification QR code keep the certificate tied to its source.
Certificates issued to a brand carry the client’s logo and name as a watermark, alongside the accession, the lot, the SHA-256 hash and a QR code to the live record. A certificate for one client cannot be passed off as another’s, and one lot’s result cannot be reused for the next.
Public verification exposes altered certificates. Report suspected misuse so our team can investigate and act.
Fake and altered certificates are the largest problem in third-party testing: a real lab’s name on a document the lab never issued. Because every Gold Standard record is public and hash-bound, a forged or edited PDF fails verification on the spot, which removes most of that risk before anyone has to act. Our counsel acts on every fake or altered certificate and every unlicensed use of the Gold Standard name or mark: takedown notices to marketplaces and registries, notice to payment processors, public misuse notices on the record, and claims under the Lanham Act and the Texas Deceptive Trade Practices Act. Vendors who test with us are protected by it; those who counterfeit it are not.

Report a certificate that does not verify, or suspected misuse of our mark, to team@goldstandardanalytics.com.
Missed quoted turnaround, or a materially contradicted result on a qualifying retest? The affected panel’s testing fee is refunded in full.
The result guarantee requires an ISO/IEC 17025-accredited laboratory to retest the same retained sample using a comparable validated method. Samples are retained 90 days so this is checkable.
Applies to every client and sample size. Sterility has a 14-day incubation and preservative efficacy a 28-day challenge; the quoted date accounts for those method requirements. The clock starts at receipt, not order. Full guarantee terms.
Swipe through the three steps →
Your accession receipt has the quoted report date. A late signed certificate triggers an automatic refund.
Within 90 days, request retained material for an accredited lab to retest using a comparable validated method.
A material contradiction means a panel-fee refund, with both results published under the accession.
Every sample enters through the carrier scan so the chain of custody starts before we touch it and intake follows one procedure. Order first; the prepaid UPS label is provided at submission. To visit the laboratory, schedule an appointment.
Short articles from the bench on how the tests work and what a certificate tells you.
Email team@goldstandardanalytics.com or call 346 770 3170, 10 AM–4 PM CST.
Invoice at submission. Prepaid UPS label available at submission.