Received, labelled, and booked in under reference
What we test
Every test is tied to a written method and a qualified instrument. Ask for a single answer, or the whole release picture in one pass.
Received, labelled, and booked in under reference
How the menu works
Each test runs within an agreed scope, on a validated method, with every figure traceable to a reference standard and kept on file for seven years. Turnaround is confirmed in your quote before anything starts.
The right structure and the right mass — confirmed, and told apart from close look-alikes.
We pull the real compound apart from everything else and report each impurity as a share of the whole.
Actual content measured against a traceable reference — the number in the vial, not on the label.
Leftover water by direct titration — it quietly changes true content and mass balance.
Counter-ion and process solvents that shift how much compound is actually present.
Trace catalyst residues and heavy metals, element by element, down to parts per million.
Bacterial endotoxin and recoverable microbial growth for anything meant to be injectable.
Sterility for material presented in an injectable format.
How identity, purity and content hold up under defined storage conditions.
Building a fit-for-purpose method when a compound is new to us.
Proving a method does what it’s meant to, on protocol.
Isolating an individual impurity and working out exactly what it is.
Tell us the compound and what you need to know. We’ll confirm scope, price and how to ship.
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