For Clinical Labs
In today’s diagnostic landscape, laboratories must deliver fast, reliable, and cost-effective results despite staffing shortages, tighter regulations, and rising technical complexity.

Validation Manager saves a lot of your time in data management and analysis, as well as in reporting your validations and verifications. But even if you know that you will save weeks of time, it can still feel frustrating if you find yourself repeating same actions on your computer. Here’s a few tips on how to reduce the repetitive work.
When you start validations, you need to plan, what kind of tests and instruments will be involved, what kind of samples will be used, and how extensive protocols will be conducted. Often you also need to decide the limits in which the results must be to be acceptable.
Validation Manager uses this information in creating your report. Filling the plan does not take much time if you have already decided what to do. But if you need to fill pretty much the same information that is already filled in some other study, it’s not so much fun to have to do it all again. To avoid that, you can copy the plan of another study when you are adding the study on your project.
This can be handy e.g. when:
Sometimes you may have a need to use the same data on multiple studies. Possible use cases include:
In Validation Manager, you can use data from another study within the same project. To keep the workflow simple, all data from the selected study is included. That’s why we recommend to reuse data only in studies using similar protocols. In case not all data is needed in the new study, your study plan settings and design selections determine which parts of the data (e.g. which methods) will be included in the report.
To give a little more flexibility for reusing data, there is also a new tool for excluding groups of results with common properties (e.g. data from certain result ranges) so that they will not be shown on the study report.
When establishing Limit of Detection using Probit approach (Analytical Sensitivity study), or Linearity or Accuracy of a quantitative method, Validation Manager needs information about sample concentrations to be able to calculate your results. You probably have this information collected in one place, so you can easily copy paste this table into Validation Manager. Click the Import samples button on Samples page to do this.
If you have only planned your study but you don’t yet have data for these samples, you should import a table giving also information about sample matrices and types in their own columns.
If you have already imported data for these samples, or they have been used in another study within the same project, columns for sample type and matrix are not necessary, as this information is already stored in Validation Manager. So you can just import sample names and concentrations.
You can use same samples in multiple studies within the same project, but concentration information is study specific. This is because sometimes the studies are conducted successively, and the analyte concentrations in samples may change in time.
Pro tip: Did you know, that though the concentration information is only used in the mentioned studies, this sample import feature is available in all studies? You can use it for prefilling or editing sample information. That way you don’t need to worry about sample types and matrices during data import.
As you’ve got this far with this article, we’ll give you one more tip:
Are you verifying a set of instruments? We advise you to import data using LIS or middleware or instrument files if a suitable integration is available. If that is not possible, we also offer you a chance to import data from multiple instruments at a time using one Excel file.
Are you interested in learning more about the ways Validation Manager can make your validations and verifications more pleasant? Please see also our article 4 steps towards smoother validations.