The impurity hiding underneath the parent peak
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…
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Everything filed in January 2024, the month of Volume 1, Number 1. The issue itself — cover, editor’s letter and table of contents — is here.
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 route did not close because of a rule about peptides.
A design note rather than a result: what the comparator was, and what that permits you to conclude.
Efficacy was never the question in this appraisal. Duration of treatment was.
Lot-level verification with a public report is a real and achievable thing. It exists in this market, on a minority of listings.
A unit is a volume. A dose is a mass. The bridge between them is concentration, and concentration is a number somebody has to calculate.
The evidence base is thin and the document says so, which is to its credit.
A design note rather than a result: what the comparator was, and what that permits you to conclude.
Efficacy was never the question in this appraisal. Duration of treatment was.
Reported from the sessions, and from the two hours afterwards.
The Journal does not treat a badge as evidence and states so wherever it reports one.
The panel drawn during a week of vomiting is measuring the vomiting.
Efficacy was never the question in this appraisal. Duration of treatment was.
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.
A proper account of an operation that existed, and of what closing it cost.
Three randomised withdrawal designs have tested what happens when treatment stops. Their results are consistent and they are consistently misreported.
Where two methods disagree, the conservative convention is to report the lower figure. It is not universal, and whether a laboratory follows it belongs on the report.
A proper account of an operation that existed, and of what closing it cost.
The route did not close because of a rule about peptides.
Documentation practice is the only part of vendor quality a buyer can assess before purchase.
Weight loss reduces bone mineral density at load-bearing sites. Whether that translates into fractures in this population is unmeasured.
Selectivity, potency and efficacy are three different measurements. The trade routinely reports none of them.
The Journal does not treat a badge as evidence and states so wherever it reports one.
A proper account of an operation that existed, and of what closing it cost.
The evidence base is thin and the document says so, which is to its credit.
Follow the resin, not the catalogue.
Reported from the analysis, not from a warning notice.
Every instrument specification quoted in an advertisement is a best case obtained on a calibration mixture, not on a submitted vial.
The route did not close because of a rule about peptides.
A proper account of an operation that existed, and of what closing it cost.
Documentation practice is the only part of vendor quality a buyer can assess before purchase.
Reported from the analysis, not from a warning notice.
Cost is the modal reason for discontinuation in every dataset we have seen, and it is absent from the clinical literature.
A rotation scheme that is too complicated will not be followed. We describe the simple ones that are.
Reported from the sessions, and from the two hours afterwards.
The report states the gradient, the wavelength and the integration threshold, which is more than most.
A design note rather than a result: what the comparator was, and what that permits you to conclude.
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.
Roughly four to seven per cent of trial participants discontinued for adverse events, mostly gastrointestinal, mostly during escalation. That is the empirical size of the…