ISO/TS 20993:2006 describes a process by which a manufacturer can identify the biological hazards associated with medical devices, estimate and evaluate the risks, control these risks and monitor the effectiveness of the control.
Status: WithdrawnPublication date: 2006-08
Edition: 1Number of pages: 4
Technical Committee: ISO/TC 194 Biological and clinical evaluation of medical devices
- ICS :
- 11.100.20 Biological evaluation of medical devices
ISO/TS 20993:2006Stage: 95.99
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