Digital process chains in industrial medical technology - Production of custom-made devices
€145.80
Retesting of active medical devices in medical use - Testing principles
€169.86
Reprocessing hazards - Risk management in reprocessing of medical devices - Trainings
€83.76
Management of hygienically relevant surfaces in medical facilities - Classification and design of hygienically relevant surfaces - Classification
€192.76
Management of hygienically relevant surfaces in medical facilities - Classification and design of hygienically relevant surfaces - Design notes for different risk classes
€112.85
Medical device software - Medical SPICE - Recommendations for software development
€153.15
Medical device software - Medical SPICE - Process assessment model
€384.00
Clinical evaluation of medical devices
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Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) - Amendment 1: Climate action changes (ISO 15378:2017/Amd 1:2024)
IEC 60601-1:2026 SER Medical electrical equipment - ALL PARTS
€7,750.00
IEC 60601-1:2005 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
€551.00
IEC 62304:2006 Medical device software - Software life cycle processes
€441.00
IEC 60601-1-8:2006 Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
IEC 60601-1-9:2007 Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design
€244.00
IEC 60601-1-10:2007 Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers
€302.00