Abstract
PreviewISO 14937:2009 specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process for medical devices.
It applies to sterilization processes in which microorganisms are inactivated by physical and/or chemical means and is intended to be applied by process developers, manufacturers of sterilization equipment, manufacturers of medical devices to be sterilized, and organizations responsible for sterilizing medical devices.
ISO 14937:2009 specifies the elements of a Quality Management System which are necessary to assure the appropriate characterization of the sterilizing agent, development, validation and routine monitoring and control of a sterilization process.
-
Status: PublishedPublication date: 2009-10
-
Edition: 2Number of pages: 37
-
- ICS :
- 11.080.01 Sterilization and disinfection in general
Buy this standard
| Format | Language | |
|---|---|---|
| std 1 166 | ||
| std 2 166 | Paper |
- CHF166
Life cycle
-
Previously
WithdrawnISO 14937:2000
WithdrawnISO 14937:2000/Cor 1:2003
-
Now
Got a question?
Check out our FAQs
Opening hours:
Monday to Friday - 09:00-12:00, 14:00-17:00 (UTC+1)