This activity consists of an effective audit of the sterilisation process to verify that it meets all regulatory standards.

During the audit, aspects such as the management of equipment validations and microbiological controls, the condition and maintenance of the equipment, the quality of the water and detergents used, the application of operating procedures for the organisation of the different phases of the sterilisation process will be considered.

The audit will be followed by the production of a gap analysis report, aimed at identifying all the aspects for improvement that can be implemented, guaranteeing the safety of the process and preserving the optimal functioning of the equipment, surgical instruments and containers.

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