Independent analysis puts a MKM liraglutide lot at 96.2%, against 94.9% on the certificate
The Journal submitted the sample and paid for the analysis. The vendor was told in advance.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 15 of 27 of this archive, newest first.
The Journal submitted the sample and paid for the analysis. The vendor was told in advance.
The result is unremarkable. What the report omits is not.
An orthogonal method separates on a different physical principle, so that species co-eluting in the first are likely to resolve in the second. Two runs of the same method at…
The result is unremarkable. What the report omits is not.
The report states the gradient, the wavelength and the integration threshold, which is more than most.
The result is unremarkable. What the report omits is not.
The interval between manufacture and analysis is the most under-read figure on the page, and the one most likely to matter by the time a vial is opened.
A reminder that a purity figure is the output of a method, and that methods differ.
The header identifies the batch, the table records the tests, and the footer says who is answerable. Two of the three are usually incomplete.
System suitability is the set of checks demonstrating that the instrument and method were performing adequately when your sample was injected. It is recorded as a matter of…
Lot-level verification with a public report is a real and achievable thing. It exists in this market, on a minority of listings.
The two ionisation techniques in general use produce different charge distributions, different adducts and different failure modes. Certificates almost never say which was…
The report states the gradient, the wavelength and the integration threshold, which is more than most.
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.
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.
The limit for a parenteral product is calculable from the dose and the body weight in two lines. Almost nobody in this trade performs the calculation.
The report states the gradient, the wavelength and the integration threshold, which is more than most.
The result is unremarkable. What the report omits is not.
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.