A written protocol that describes what is to be accomplished should be prepared
[5]. It should specify the data to be collected, the number of batches to be
included in the study, and how the data, once assembled, will be treated for
relevance. The criteria for acceptable results should be described. The date of
approval of the protocol by the validation organization should also be noted.
The value of a protocol is to control the direction of the study, as well as provide
a baseline in the event unanticipated developments necessitate a change in strategy.
A written protocol is also an FDA recommendation
validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medicinal product meeting its pre-determined specifications and quality attributes
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Pharmaceutical Validation Documentation Requirements
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