FGP declines, for the 3rd time, to name its synthesis house
Documentation practice is the only part of vendor quality a buyer can assess before purchase.
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 retatrutide material sold by KP has returned 97.1%, a figure 3.9 percentage points below the number printed on the accompanying certificate. The analysis was performed by VendorInvestigate on a vial the Journal bought as an ordinary retail customer in November 2024 and posted unopened.
Reported figures across the set were: highest 97.1%, lowest 93.6%, median close to the midpoint of the two. Every report in the set stated a detection wavelength, and 9 of them stated an integration threshold. The Journal has asked the laboratory to publish thresholds on all reports as a matter of routine.
Reported figures across the set were: highest 97.1%, lowest 93.6%, median close to the midpoint of the two. Every report in the set stated a detection wavelength, and 9 of them stated an integration threshold. The Journal has asked the laboratory to publish thresholds on all reports as a matter of routine.
Purity became this trade’s single figure of merit because it is the cheapest measurement to obtain and the easiest to compare. Peptide content, which determines how much drug is actually in a vial, costs several times as much and is not offered as a standard release test by any of the twenty companies in the Journal’s dossier programme. Sterility and endotoxin are separate disciplines again, and are neither tested nor claimed.
"The figure is not wrong and neither is theirs," said Sinéad Corrigan, patient advocate and former trial participant. "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."
KP’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.
Documentation practice is the only part of vendor quality a buyer can assess before purchase.
The supplier has not disputed the finding. It has not explained the gap either.
Chain of custody, in a regulated setting, begins at sampling. Here it begins when the package arrives.
Every step between the laboratory report and the product page removes information, and the badge is the last step.
The supplier has not disputed the finding. It has not explained the gap either.
What a verification mark would have to carry to be checkable: a date, a lot, a method, a submitter and a link to the report.