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Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008)
99.60 Withdrawal effective
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013)
99.60 Withdrawal effective
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)
99.60 Withdrawal effective
Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)
99.60 Withdrawal effective
Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)
99.60 Withdrawal effective
Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005/Amd 1:2013)
99.60 Withdrawal effective
Clinical investigation of medical devices for human subjects - Part 1: General requirements (ISO 14155-1:2003)
99.60 Withdrawal effective
Clinical investigation of medical devices for human subjects - Part 1: General requirements (ISO 14155-1:2003)
99.60 Withdrawal effective
Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
99.60 Withdrawal effective
Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
99.60 Withdrawal effective
Clinical investigation of medical devices for human subjects - Good clinical practice - Technical Corrigendum 1 (ISO 14155:2011/Cor 1:2011)
99.60 Withdrawal effective
Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003)
99.60 Withdrawal effective
Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003)
99.60 Withdrawal effective
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2000)
99.60 Withdrawal effective
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2000)
99.60 Withdrawal effective
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006)
99.60 Withdrawal effective
Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for the active (including active implantable) medical device industry
99.60 Withdrawal effective
Medical electrical equipment - Part 1: General requirements for safety
99.60 Withdrawal effective
