The Distinction Standards Audit Tool for Reprocessing and Sterilization of Reusable Medical Devices is evidence-informed standards developed in consultation with stakeholders from across Canada and include elements from CSA standards. These standards are divided into the following sections:
- Medical device reprocessing service design
- Training, education, and competency
- Medical device reprocessing department design
- Policies, procedures, and manufacturer’s instructions
- Occupational health and safety requirements
- Computerized inventory management system
- Selection, installation, and maintenance of reprocessing equipment and medical devices
- Cleaning and disinfection of medical devices
- Sterilization of medical devices
- Storage and transportation of medical devices
- Recall procedures
- Risk and quality management