This standard specifies a process for manufacturers to identify hazards associated with medical devices, including in vitro diagnostic (IVD) medical devices, estimate and evaluate associated risks, control those risks, and monitor the effectiveness of controls. The requirements of this standard apply to all stages of the medical device life cycle. This standard is not intended for clinical decision-making. This standard does not specify acceptable risk levels. This standard does not require manufacturers to have an appropriate quality system in place. However, risk management can be an integral part of the quality management system.
YY/T 0316-2008 history
2016YY/T 0316-2016 Medical devices.Application of risk management to medical devices
2008YY/T 0316-2008 Medical devices.Application of risk management to medical devices
2003YY/T 0316-2003 Medical devices-Application of risk management to medical devices