Designing Medical Sterilisation and Disinfection Protocols

Course Overview

Variation in medical sterilisation protocols between shifts and sites is where avoidable harm lives. The data supporting the practice within health and pharmaceutical services is usually present but rarely assembled into a decision. It suits anyone whose decisions touch the health and pharmaceutical services discipline, in large organisations and small ones alike. Content is organised around the decisions practitioners actually face in medical sterilisation protocols, not around theory headings. Participants gain a realistic view of what this area of health and pharmaceutical services costs and what it returns. Practitioner evidence points the same way: the health and pharmaceutical services capability improves fastest where responsibility for it is named and owned. Buying a tool rarely fixes medical sterilisation protocols; the underlying capability has to be built internally first. Participants apply this part of health and pharmaceutical services to their own clinical service throughout, so the output is directly usable. Participants leave with a plan for the wider health and pharmaceutical services agenda sized to what their organisation can realistically absorb.