Guidelines and standards
Professional guidance and reference materials supporting consistent sterile processing practice.

SPAG Knowledge Centre
Explore trusted public resources that support sterile processing education, quality improvement and professional development.
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Professional guidance and reference materials supporting consistent sterile processing practice.
Learning materials, technical references and tools for ongoing professional development.
Association publications and relevant updates for Ghana's sterile processing community.
Resource library
Browse materials approved by SPAG for public professional use.
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Guidelines and standards
ISO 17665:2024 specifies requirements for the development, validation and routine control of moist-heat sterilization processes for medical devices. The standard addresses the controlled and monitored application of moist heat to achieve reliable sterilization and is relevant to organizations and facilities responsible for medical-device sterilization. SPAG provides this link to the official ISO record; access to the complete standard is subject to ISO's licensing and purchase requirements.
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Open Member HubEducation resources
This FDA educational resource provides a straightforward overview of how reusable medical devices are reprocessed between patient uses. It explains the general three-stage pathway beginning with point-of-use treatment, followed by thorough cleaning in the reprocessing area and then appropriate disinfection or sterilization based on the device's intended use and construction. It is a useful introductory resource for students and new sterile processing personnel.
Guidelines and Standards
This CDC guideline provides evidence-based recommendations for cleaning, disinfection and sterilization in healthcare facilities. It addresses medical-device classification, cleaning, chemical disinfectants, sterilization technologies, steam and low-temperature sterilization, sterilizing practices, monitoring and other important infection-control considerations. It serves as an important reference for sterile processing and infection prevention professionals.
Guidelines and Standards
This WHO guidance manual provides comprehensive information on the decontamination and reprocessing of reusable medical devices in healthcare facilities. It covers sterile services infrastructure and staffing, cleaning, preparation and packaging, chemical disinfection, endoscope reprocessing, sterilization, transportation of medical devices and related quality and safety considerations. It is a valuable reference for sterile processing personnel, healthcare managers, infection prevention professionals and facilities seeking to strengthen their medical-device reprocessing practices.