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#qualitycontrols

I have transitioned to a new instrument or method within the DKD program. What actions should be taken?

By what procedure and within what period may participants lodge an appeal against their results?

How can participants access transparency regarding the assigned value, and how is this value determined?

What are the critical rules regarding the preparation, reconstitution, and stability period of lyophilized samples?

What is included in the participant reports, and which analytical tools are made available to users?

How does the Chauvenet outlier test used in the analysis of participant results work?

What types of checks does the Serocon Portal apply during data entry, and which errors does it prevent?

What distinguishes the Z-score from the Z′-score, and under what circumstances should the Z′-score be applied?

By which methods and under what conditions are statistical evaluations conducted in DKD programs?

How are homogeneity and stability analyses of samples performed, and according to which standard are they approved?

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