What changed after we published the first version of this
None of what this piece asks for is commercially sensitive, and all of it is already known to whoever released the batch.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Testing Dispatch
The result is unremarkable. What the report omits is not.
An independent purity determination on tirzepatide material sold by FGP has returned 96.0%, a figure 2.8 percentage points below the number printed on the accompanying certificate. The analysis was performed by Medutest on a vial the Journal bought as an ordinary retail customer in May 2026 and posted unopened.
The Journal purchased 4700 vials from the same lot and had 7 of them analysed separately, in order to distinguish vial-to-vial variation from method variation. Vial-to-vial agreement was within 0.4 percentage points. Method-to-method disagreement was an order of magnitude larger.
The Journal purchased 4700 vials from the same lot and had 7 of them analysed separately, in order to distinguish vial-to-vial variation from method variation. Vial-to-vial agreement was within 0.4 percentage points. Method-to-method disagreement was an order of magnitude larger.
Four independent services — Medutest, VendorInvestigate, and the two others operating in this market — carry the analytical burden for a trade that has no release-testing obligation of its own. Each is paid by whoever submits the sample, which is usually the vendor. The Journal’s position is that a submitter-pays model is workable but that its incentive structure has to be stated whenever a result is quoted as verification.
"The figure is not wrong and neither is theirs," said Havel Novotný, independent laboratory quality manager. "They are answers to two different questions and the trade has decided to pretend there is only one question. Print the gradient and the argument disappears."
FGP’s dossier has been updated with this determination and with the date of the request for comment. The dossier’s "what we could not verify" box records the questions still outstanding.
None of what this piece asks for is commercially sensitive, and all of it is already known to whoever released the batch.
Nothing on this page is difficult. It is simply unfamiliar, and unfamiliarity is what makes a weak certificate look like a strong one.
Every step between the laboratory report and the product page removes information, and the badge is the last step.
Documentation practice is the only part of vendor quality a buyer can assess before purchase.
What happens to traceability when bulk material is subdivided, repackaged and relabelled two or three times before sale.
The supplier has not disputed the finding. It has not explained the gap either.