Controls specified to your device and your cost target.
Standard catalogue material rarely fits a point-of-care platform exactly. We build the control around the assay it has to verify.
According to your requirements
Filling volumes
Vial and bulk volumes matched to how your device consumes control material and how often it is run.
Target values and levels
Levels positioned where they are clinically useful for your assay, with target values assigned per lot.
Single or multi-analyte
One analyte per control, or a combined control covering several analytes in a single vial.
Parameters removed
Leaving out parameters you do not need improves cost efficiency without weakening the check that matters.
From requirement to series supply
Requirements
You describe the device, analytes, levels and volumes, and any documentation you need with each lot.
Specification
We propose a formulation, matrix, level design and target value strategy, and confirm feasibility.
Pilot lot
A first lot is produced and tested for stability and homogeneity, and evaluated on your platform.
Series supply
Repeat lots follow the agreed specification with consistent target values and defined release limits.
Pay for the parameters you use
Removing unnecessary parameters lowers the cost per lot and simplifies evaluation. A programme that only needs CRP and glucose should not be paying for analytes it never reports, and a device with a narrow measuring range does not need levels outside it.
The result is a control that is cheaper to run, quicker to interpret and still fully defensible: human matrix, verified stability, homogeneity to ISO 13528 and release against Rilibäk total allowable error limits.
Send us your specification →