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 This protocol needs an intensive & planned set of activities. It establishes proof that every cleaning method Employed in an organization is constantly helpful. It includes using committed products for demanding screening & documentation. The utmost acceptable residue limitations should be established based upon the safety and regulatory needs.

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It will involve accumulating and evaluating data on all aspects and levels in the manufacturing process. This includes:Developing documented proof just before process implementation that a procedure does what it proposed to carry out based on preplanned protocols. This method of validation is Ordinarily undertaken Any time the process for the new m

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