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The IEC Phase 7 deals with overall validation planning.
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The overall validation design was composed of two distinct evaluations.
To this regard, the overall validation activities should be described in a general document, usually known as Validation Master Plan VMPP).
Overall, validation data suggested that the assay was precise, reproducible, and sensitive for sample testing.
Tumors may shrink during histological processing, which further complicates the overall validation process [9].
Overall, validation analyses showed that the two instruments were comparable.
The overall validation process is shown in Figure 2.
Validation activities should be planned in a validation plan, in an orderly manner.
First, a validation plan must be developed.
It drives the development of the assay analytical validation plan.
A prespecified validation plan was used to check for plausibility.
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