Medutest result on a Hangzhou liraglutide lot lands 4.1 points below the supplier’s figure
A reminder that a purity figure is the output of a method, and that methods differ.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 17 of 68 of this archive, newest first.
A reminder that a purity figure is the output of a method, and that methods differ.
The masking phenomenon known as low endotoxin recovery means a formulation can return a clean result while containing endotoxin the assay cannot see.
A design note rather than a result: what the comparator was, and what that permits you to conclude.
The document is four pages. Three of them are about dates.
Reported from the sessions, and from the two hours afterwards.
Reported from the analysis, not from a warning notice.
Three randomised withdrawal designs have tested what happens when treatment stops. Their results are consistent and they are consistently misreported.
The Journal does not treat a badge as evidence and states so wherever it reports one.
Follow the resin, not the catalogue.
The evidence base is thin and the document says so, which is to its credit.
Reported from the sessions, and from the two hours afterwards.
Reported from the analysis, not from a warning notice.
Receptor expression maps explain the effect profile better than any dose-response curve.
A badge asserts that something was tested. It does not assert what, when, on whose sample, by what method, or whether the lot on sale is the lot that was tested.
Reported from the sessions, and from the two hours afterwards.
The evidence base is thin and the document says so, which is to its credit.
Reported from the analysis, not from a warning notice.
Lot-level verification with a public report is a real and achievable thing. It exists in this market, on a minority of listings.
A survey of what the meta-analyses support, with the populations named.
The observation that closes a facility is rarely the dramatic one.
The evidence base is thin and the document says so, which is to its credit.
Documentation practice is the only part of vendor quality a buyer can assess before purchase.
Reported from the analysis, not from a warning notice.
Severity in these tables is graded by interference with activity, not by how unpleasant the experience was. Those are different measurements.
A purity figure is silent on peptide content, on water, on counter-ion, on sterility, on endotoxin and on stability. Each of those silences has a price attached.
Trial adverse-event tables count episodes reported to a study nurse. They are the best data we have and they systematically under-record the mundane.
A proper account of an operation that existed, and of what closing it cost.
The document is four pages. Three of them are about dates.
Documentation practice is the only part of vendor quality a buyer can assess before purchase.
Efficacy was never the question in this appraisal. Duration of treatment was.