ISO/TS 20993:2006
$12.35
Biological evaluation of medical devices — Guidance on a risk-management process
| Published By | Publication Date | Number of Pages |
| ISO | 2006-08 | 10 |
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.
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