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Defining quality in the sterile processing department (SPD) is a challenge for many healthcare organizations and hospitals. Most of the time spent on sterile processing is not about improvement but about fighting turnover and doing damage control when delays or errors occur. However, when quality is quantified and measured, the SPD can improve by leaps and bounds, diminishing risk and increasing OR revenue.
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Table of Contents The Critical Importance of Medical Device Sterilization Common Methods of Medical Device Sterilization Steam Sterilization (Autoclaving) Ethylene Oxide (EtO) Sterilization Low-Temperature Hydrogen Peroxide Sterilization Radiation Sterilization Sterilization Validation and Monitoring Biological Indicators Chemical Indicators Physical Monitoring Regulatory Framework and Standards FDA Oversight International Standards Healthcare Facility Accreditation Challenges in Medical Device
Defining quality in the sterile processing department (SPD) is a challenge for many healthcare organizations and hospitals. Most of the time spent on sterile processing is not about improvement but about fighting turnover and doing damage control when delays or errors occur. However, when quality is quantified and measured, the SPD can improve by leaps and bounds, diminishing risk and increasing OR revenue.
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