11.080.01 Sterilization and disinfection in general

BS EN ISO 11737-2. Sterilization of medical devices. Microbiological methods Part 2. Tests of sterility performed in the definition, validation and maintenance of a sterilization process

BS EN ISO 14160. Sterilization of health care products. Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives. Requirements for characterization, development, validation and routine control of a sterilization process for medical devices

BS EN ISO 13408-6. Aseptic processing of health care products Part 6. Isolator systems

BS ISO 17664-2. Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices Part 2. Non-critical medical devices

BS EN ISO 11737-1 AMD1. Sterilization of health care products. Microbiological methods Part 1. Determination of a population of microorganisms on products

Sterilization of medical devices. Requirements for medical devices to be designated "STERILE" Requirements for terminally sterilized medical devices

Sterilization of medical devices. Requirements for medical devices to be designated "STERILE" Requirements for aseptically processed medical devices

Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices

Sterilization of health care products. Radiation Requirements for development, validation and routine control of a sterilization process for medical devices

Sterilization of health care products. Radiation Establishing the sterilization dose

Sterilization of health care products. Radiation Guidance on dosimetric aspects of development, validation and routine control

Sterilization of health care products. Biological indicators General requirements