11.100.20 - Biological evaluation of medical devices
Showing 17–32 of 246 results
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ISO 22442-1:2020
Medical devices utilizing animal tissues and their derivatives — Part 1: Application of risk management…
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ISO 22442-1:2015
Medical devices utilizing animal tissues and their derivatives — Part 1: Application of risk management…
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ISO 22442-1:2007
Medical devices utilizing animal tissues and their derivatives — Part 1: Application of risk management…
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ISO 20776-2:2021
Clinical laboratory testing and in vitro diagnostic test systems – Susceptibility testing of infectious agents…
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ISO 20776-2:2007
Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents…
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ISO 20776-1:2019
Sensibilité in vitro des agents infectieux et évaluation des performances des dispositifs pour antibiogrammes —…
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ISO 20776-1:2006
Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents…
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ISO 17593:2007
Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems…
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ISO 17593:2022
Clinical laboratory testing and in vitro medical devices – Requirements for in vitro monitoring systems…
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ISO 14155:2020
Clinical investigation of medical devices for human subjects — Good clinical practice Published By Publication…
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ISO 14155:2011
Clinical investigation of medical devices for human subjects — Good clinical practice Published By Publication…
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ISO 14155-2:2003
Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans Published…
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ISO 14155-1:2003
Clinical investigation of medical devices for human subjects — Part 1: General requirements Published By…
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ISO 13022:2012
Medical products containing viable human cells — Application of risk management and requirements for processing…
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ISO 10993-9:2019
Évaluation biologique des dispositifs médicaux — Partie 9: Cadre pour l’identification et la quantification des…
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ISO 10993-8:2000
Biological evaluation of medical devices — Part 8: Selection and qualification of reference materials for…