Validation phase for automation
Once the system is working correctly from a technical point of view, it is necessary to evaluate system performance from an analytical and operational point of view.
Therefore a carefully planned validation protocol is carried out.

The protocol uses preset performance criteria and is carried out in accordance to international reference methods, such as ISO 17025. Reference materials, standards and samples are provided by the customer. The validation is usually carried out on-site in our own labs (factory acceptance) as well as on-site (site acceptance).

All data are evaluated statistically. If required, minor adjustments are carried out. Significant hardware adjustments are generally not necessary due to the detailed
assessment phase.


Our Services

Our services are tailored to suit all your sample preparation needs:

   •   Feasibility study
   •   System integration
   •   Process analysis
   •   Advice & consultancy
   •   Validation (CE mark)

Our specialists are available to answer all your questions.

Oil and Fat Seminar

The FAME PAL series, developed by SampleQ some years ago, is our proven solution for automatic derivatization of fatty acids to fatty acids methyl esters.

Based on this experience, our team has co-created a similar solution for the analysis of 3-MCPD and glycidyl esters in edible oils in collaboration with our customers in the Netherlands.

For more information please participate (by clicking on the link)

Subscribe here...    


We provide intense training programs for new as well as experienced users.

Not only proper system operation, but also troubleshooting and maintenance are dealt with in great detail.