ISO/TS 20993:2006 PDF
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Biological evaluation of medical devices — Guidance on a risk-management process
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.
| Edition | 2006 |
|---|---|
| Published Date | 2006 |
| Published By | ISO/TS |
| Page Count | 4 |
