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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, ]
• [25] Water for Operating Washer-Disinfectors
  [PDF File, ]
• [26] Water for Operating Washer-Disinfectors (Part 2)
  [PDF File, ]
• [27] Packaging Systems
  [PDF File, ]
• [28] Daily Check of Washer-Disinfectors Before Placing Them in Operation
  [PDF File, ]
• [29] Verification of the Performance of Washer-Disinfectors Used for Thermal Disinfection
  [PDF File, ]
• [30] Packaging Systems - Part 2: Hard Packaging
  [PDF File, ]
• [31] Updating the Decision Tree on Risk Assessment and Classification of Medical Devices
  [PDF File, ]
• [32] How Quality Management is Structured in CSSD Practice
  [PDF File, ]
• [33] Mesh Trays and Their Implications for Successful Cleaning in the Washer-Disinfector
  [PDF File, ]
• [34] Packaging Part 3: Summary
  [PDF File, ]
• [35] Loading Pattern and Its Implications for Successful Cleaning in the Washer-Disinfector
  [PDF File, ]
• [36] Risk Management in the CSSD
  [PDF File, ]
• [37] Guide to Compilation of Standard Operating Procedures
  [PDF File, ]
• [38] Checklist for Preparation of Visits by the Competent Inspection Authorities
  [PDF File, ]
• [39] Recommendations for the Storage Period for Sterile Medical Devices
  [PDF File, ]
• [40] Automated Processing of Ophtalmologic Instruments
  [PDF File, ]
• [41] Production of Heat Sealing Seams for Packing Medical Devices (based on the currently valid standards, ISO 11607, EN 868, DIN 58953)
  [PDF File, ]
• [42] Using Process Challenge Devices To Verify Cleaning Performance for Validation of Washer-Disinfector Processes
  [PDF File, ]
• [43] Recommendations for Validation of Steam Sterilisation Processes in Large Sterilisers
  [PDF File, ]
• [44] Compilation of Procedures
  [PDF File, ]
• [45] Decontamination of Narrow-Lumened Medical Devices
  [PDF File, ]
• [46] Manufacturer's Instructions for Decontamination
  [PDF File, ]
• [47] Insights Gleaned from Workshops at the 10th DGSV Congress: Manufacturer's Instructions for Decontamination
  [PDF File, ]
• [48] Decontamination of Plastic Medical Devices or of Devices with Plastic Components (Part 1)
  [PDF File, ]
• [49] Decontamination of Plastic Sterilisation Containers and Plastic Supports
  [PDF File, ]
• [50] Requirements for Construction or Conversion of a Hospital Central Sterile Supply Department
  [PDF File, ]
• [51] Decontamination of Anaesthesia and Respiratory Accessories
  [PDF File, ]
• [52] Requirements for Construction or Conversion of a Hospital Central Sterile Supply Department Part 2 - Staff and Material Routes
  [PDF File, ]
• [53] Verification of Completeness of Validation Protocols for WD Processes
  [PDF File, ]
• [54] Performance Requalification for No Particular Reason
  [PDF File, ]
• [55] Performance Requalification on Changing the Process Chemicals
  [PDF File, ]
• [56] Decontamination of Motor Systems
  [PDF File, ]

^* Quality Task Group = Arbeitskreis Qualität (AK "Qualität")