Comment Closes On
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Committee
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LBI/36/1 |
Document Type
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Draft |
ISBN
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|
Pages
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Published
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|
Publisher
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British Standards Institution
|
Status
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Superseded |
Superseded By
|
|
ISO 11137-1:2006
|
Sterilization of health care products Radiation Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices |
EN 550 : 1994
|
STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF ETHYLENE OXIDE STERILIZATION |
ISO 14644-6:2007
|
Cleanrooms and associated controlled environments Part 6: Vocabulary |
ISO 14644-8:2013
|
Cleanrooms and associated controlled environments Part 8: Classification of air cleanliness by chemical concentration (ACC) |
ISO 14644-2:2015
|
Cleanrooms and associated controlled environments Part 2: Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration |
ISO 14644-5:2004
|
Cleanrooms and associated controlled environments — Part 5: Operations |
ISO 14644-3:2005
|
Cleanrooms and associated controlled environments Part 3: Test methods |
ISO 14644-7:2004
|
Cleanrooms and associated controlled environments — Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments) |
ISO 14644-1:2015
|
Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
ISO 14644-4:2001
|
Cleanrooms and associated controlled environments — Part 4: Design, construction and start-up |
EN 980:2008
|
Symbols for use in the labelling of medical devices |
ISO 17665-1:2006
|
Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices |
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