2iso |
2009-11-25 23:49 |
BS EN ISO 14971:2009
*New* Medical Devices. Medical devices. Application of risk management to medical devices
This standard specifies a procedure by which a manufacturer can identify the hazards associated with medical devices and their accessories, including in vitro diagnostic medical devices. It also specifies a procedure to estimate and evaluate the identified risks, control these risks and monitor the effectiveness of the control.
The requirements of BS EN ISO 14971:2009 are applicable to all stages of the lifecycle of a medical device, but do not apply to clinical judgements relating to the use of a medical device and it does not specify acceptable risk levels.
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