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The article presents the discussion on Quality assurance in the RUMED through well-targeted process monitoring where validation involving verification and evidence-based documentation of the process effectiveness.

The article presents the discussion on job description setting out tasks, powers, and competencies. Topics include management board, economic operator, RUMED management, and shift management with reference to an organigram; management of incoming contaminated medical devices destined for automated and manual cleaning or disinfection; and inspection and release of sterile supplies.

The article focuses on the use of standard operating procedure (SOPs) help to demonstrate compliance with all the hygienic and technical requirements legally specified for medical device reprocessing. Topics include SOPs describe the correct implementation of all relevant work steps in the respective workplace; and SOPs being compiled to complement a procedure for all relevant steps of the reprocessing process.

The article presents the transport and storage not adversely affecting the medical device characteristics. Topics include sterilized medical devices (MDs) being protected against contamination when transported between the reprocessing department and the site of use; using MDs harbor potentially infectious contaminants against which the must be protected; and sterilized MDs must be transported separately from non-sterilized MDs in ruling out contamination.