Why a result on one vial says less than the trade needs it to
Chain of custody, in a regulated setting, begins at sampling. Here it begins when the package arrives.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 7 of 8 of this archive, newest first.
Chain of custody, in a regulated setting, begins at sampling. Here it begins when the package arrives.
A shallow gradient resolves impurities that a steep one runs into the parent peak. Both methods are legitimate; only one of them can see the small stuff.
We set out the parameters a method disclosure would contain, all of which are known to whoever ran the sample and none of which is commercially sensitive.
The condition on arrival is recorded by some services and not others, and it is one of the more informative lines in a report.
We work through a single chromatogram twice, under two integration conventions, and show where the difference comes from.
A shallow gradient resolves impurities that a steep one runs into the parent peak. Both methods are legitimate; only one of them can see the small stuff.
Accreditation to the international competence standard covers the scope a laboratory has been assessed for, which is not necessarily the test you commissioned.
What a laboratory can and cannot know about the provenance, storage history and representativeness of what lands on its bench.
Duplicate submissions under different names test within-laboratory repeatability, which is a different quantity from between-laboratory reproducibility.
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.
We work through a single chromatogram twice, under two integration conventions, and show where the difference comes from.
The condition on arrival is recorded by some services and not others, and it is one of the more informative lines in a report.
Aggregates dissociate in the mobile phase and are recorded as monomer. Only a size-based separation reports them.
A result on one vial generalises to a batch only if the vial was drawn in a way that makes it representative — and nobody records how it was drawn.
Duplicate submissions under different names test within-laboratory repeatability, which is a different quantity from between-laboratory reproducibility.
A purity percentage is the most quoted figure in the research-peptide trade and one of the least examined. We asked four laboratories to analyse the same vial and got four…
The most useful single addition to any purity determination is a second separation under a different pH or on a different stationary phase, and the second-most useful is a…
The Journal does not treat a badge as evidence and states so wherever it reports one.
The condition on arrival is recorded by some services and not others, and it is one of the more informative lines in a report.
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.