Education - Recommendations
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General Guidelines and Recommendations
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Guidelines and Recommendations published in Central Service
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Recommendations by the Quality Task Group
- [1] Recommendations
- [2] Transport from the OR to the CSSD
- [3] Validation (Part 1)
- [4] Validation (Part 2)
- [5] Cooperation with the OR and other Departments
- [6] Deciding How to Process a New Medical Device
- [7] Validation of Older Steam Sterilisers
- [8] Cleaning and Disinfection in the Ultrasonic Bath (Part 1)
- [9] Cleaning and Disinfection in the Ultrasonic Bath (Part 2)
- [10] "Flash Sterilisation"
- [11] Programmes for Automated Processing
- [12] Programmes for Automated Processing (Part 2)
- [13] Quality Assurance on the "Clean Side" of a CSSD
- [14] Thermal Washer-Disinfectors - Investigating the Disinfection Effect with Thermologgers
- [15] Release and Storage of Medical Devices after Sterilisation
- [16] Quality Assurance on the Unclean Side of a CSSD
- [17] Quality Assurance on the Unclean Side of a CSSD (Part 2)
- [18] Bowie Dick Test
- [19] Cleaning (Part 1) - Instruments Causing Problems
- [20] Cleaning (Part 2) - Validation of Cleaning Efficacy
- [21] Why Computerised Documentation? - Reflections from the Field
- [22] Classifying Medical Devices before Processing (Part 1)
- [23] Classifying Medical Devices before Processing (Part 2)
- [24] Classifying Medical Devices before Processing (Part 3)
[PDF File, 571 KB]
- [25] Water for Operating Washer-Disinfectors
[PDF File, 523 KB]
- [26] Water for Operating Washer-Disinfectors (Part 2)
[PDF File, 744 KB]
- [27] Packaging Systems
[PDF File, 570 KB]
- [28] Daily Check of Washer-Disinfectors Before Placing Them in Operation
[PDF File, 917 KB]
- [29] Verification of the Performance of Washer-Disinfectors Used for Thermal Disinfection
[PDF File, 765 KB]
- [30] Packaging Systems - Part 2: Hard Packaging
[PDF File, 367 KB]
- [31] Updating the Decision Tree on Risk Assessment and Classification of Medical Devices
[PDF File, 284 KB]
- [32] How Quality Management is Structured in CSSD Practice
[PDF File, 533 KB]
- [33] Mesh Trays and Their Implications for Successful Cleaning in the Washer-Disinfector
[PDF File, 720 KB]
- [34] Packaging Part 3: Summary
[PDF File, 282 KB]
- [35] Loading Pattern and Its Implications for Successful Cleaning in the Washer-Disinfector
[PDF File, 992 KB]
- [36] Risk Management in the CSSD
[PDF File, 509 KB]
- [37] Guide to Compilation of Standard Operating Procedures
[PDF File, 524 KB]
- [38] Checklist for Preparation of Visits by the Competent Inspection Authorities
[PDF File, 1.3 MB]
- [39] Recommendations for the Storage Period for Sterile Medical Devices
[PDF File, 546 KB]
- [40] Automated Processing of Ophtalmologic Instruments
[PDF File, 3.4 MB]
- [41] Production of Heat Sealing Seams for Packing Medical Devices (based on the currently valid standards, ISO 11607, EN 868, DIN 58953)
[PDF File, 4.8 MB]
- [42] Using Process Challenge Devices To Verify Cleaning Performance for Validation of Washer-Disinfector Processes
[PDF File, 163 KB]
- [43] Recommendations for Validation of Steam Sterilisation Processes in Large Sterilisers
[PDF File, 79 KB]
- [44] Compilation of Procedures
[PDF File, 71 KB]
- [45] Decontamination of Narrow-Lumened Medical Devices
[PDF File, 821 KB]
- [46] Manufacturer's Instructions for Decontamination
[PDF File, 97 KB]
- [47] Insights Gleaned from Workshops at the 10th DGSV Congress: Manufacturer's Instructions for Decontamination
[PDF File, 61 KB]
- [48] Decontamination of Plastic Medical Devices or of Devices with Plastic Components (Part 1)
[PDF File, 96 KB]
- [49] Decontamination of Plastic Sterilisation Containers and Plastic Supports
[PDF File, 108 KB]
- [50] Requirements for Construction or Conversion of a Hospital Central Sterile Supply Department
[PDF File, 102 KB]
- [51] Decontamination of Anaesthesia and Respiratory Accessories
[PDF File, 82 KB]
- [52] Requirements for Construction or Conversion of a Hospital Central Sterile Supply Department Part 2 - Staff and Material Routes
[PDF File, 142 KB]
- [53] Verification of Completeness of Validation Protocols for WD Processes
[PDF File, 48 KB]
- [54] Performance Requalification for No Particular Reason
[PDF File, 55 KB]
- [55] Performance Requalification on Changing the Process Chemicals
[PDF File, 135 KB]
- [56] Decontamination of Motor Systems
[PDF File, 209 KB]
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Recommendations by Swissmedic - Swiss Agency for therapeutic products
Swissmedic - www.swissmedic.ch
- Guidelines and Recommendations in French:
- Guidelines and Recommendations in German:
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Recommendations by the Irish Health Service Executive (HSE)
© 2009 WFHSS • Updated: 17 November 2008, 10:05 [GMT]
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:: Education :: Recommendations