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• cleaning after item changeover (when one pharmaceutical formulation is currently being changed for one more, totally diverse formulation);The maximum appropriate residue limitations need to be established based on the security and regulatory prerequisites. This should be Obviously mentioned during the validation protocol.Furthermore, documents
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To describe the procedure for Evaluation of drinking water sample for estimation of the number of feasible aerobic micro-organisms existing & for the detection of Pathogenic microbial species.The data produced from these studies are fewer variable In case the cell populations are homogeneous. Liquid cultures or confluent growths on stable medium ar