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About This Item

 

Full Description

Valuable checklist also available to assist with compliance to this standard.

The requirements contained in this document provide manufacturers with a framework within which experience, insight and judgment are applied systematically to manage the risks associated with the use of medical devices.

This document was developed specifically for manufacturers of medical devices on the basis of established principles of risk management that have evolved over many years. This document could be used as guidance in developing and maintaining a risk management process for other products that are not necessarily medical devices in some jurisdictions and for suppliers and other parties involved in the medical device life cycle.

This document specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The process described in this document intends to assist manufacturers of medical devices to identify the hazards associated with the medical device, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls.

The requirements of this document are applicable to all phases of the life cycle of a medical device. The process described in this document applies to risks associated with a medical device, such as risks related to biocompatibility, data and systems security, electricity, moving parts, radiation, and usability.

The process described in this document can also be applied to products that are not necessarily medical devices in some jurisdictions and can also be used by others involved in the medical device life cycle.

This document does not apply to:
  • decisions on the use of a medical device in the context of any particular clinical procedure; or
  • business risk management.
This document requires manufacturers to establish objective criteria for risk acceptability but does not specify acceptable risk levels.

Risk management can be an integral part of a quality management system. However, this document does not require the manufacturer to have a quality management system in place.

NOTE Guidance on the application of this document can be found in ISO/TR 24971.

keywords: ISO 14971:2019;ISO 14971-2019;ISO 14971;Risk Management
 

Document History

  1. ISO 14971:2019

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    Medical devices - Application of risk management to medical devices

    • Most Recent
  2. ISO 14971:2019 Plus Redline


    Medical devices - Application of risk management to medical devices

    • Historical Version
  3. ISO 14971:2007


    Medical devices - Application of risk management to medical devices

    • Historical Version
  4. ISO 14971/Amd1:2003


    Medical devices - Application of risk management to medical devices - Amendment 1: Rationale for requirements

    • Historical Version
  5. ISO 14971:2000


    Medical devices -- Application of risk management to medical devices

    • Historical Version