This session will examine regulatory standards governing high-level disinfection and sterilization, with emphasis on how surveyors interpret and apply those requirements in acute and procedural settings. Participants will review the most frequently cited non-compliance findings, analyze underlying root causes, and explore practical corrective actions that align with CMS, CDC, and manufacturer instructions for use (IFUs). The program will also provide a framework for building sustainable monitoring and quality assurance processes to strengthen oversight, mitigate regulatory exposure, and ensure consistent adherence to infection prevention protocols.
Webinar
Seconds to contaminate, years to recover
What healthcare leaders must know about cleaning, disinfection, and sterilization
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Risk assessment sample
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