The fast bioindicador provides the approval of the cycle of sterilization from 6 hours of aeration in safe residual limits, what it provided to profit of productivity and operational security when compared with the previous time of 48 hours of conventional bioindicador 1264. CONCLUSION All the stages of the validation had been reached successfully for the qualifications physical, microbiological and chemical residual. The methodology for residual analysis GCFID was validated successfully and the residual waste demonstrated to efficiency and reprodutibilidade from the time of 6 hours of aeration for the enteral bottle, for 10 the allowed criterion of g/mL. .

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