ISO 14971: Difference between revisions
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== References == |
== References == |
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Revision as of 02:38, 12 April 2010
ISO 14971 is an ISO standard, published in 2007, that represents the requirements for a risk management system for medical devices.[1] This standard supersedes earlier documents such as ISO 14971:2000 and EN 1441.
This standard establishes the requirements for risk management to determine the safety of a medical device by the manufacturer during the product life cycle.
This standard adopted by CEN as EN ISO 14971:2007 is harmonized with respect to the European medical device directives 93/42/EEC, 90/385/EEC and 98/79/EC.[2]
The requirements of this standard should be applied to medical devices as well established in the ISO 13485 in paragraph 7.1 of planning.
See also
- List of ISO standards
- ISO 13485
- Medical technology
- Medical device
- Clinical Engineering
- Electromedicine
- System suitability test
- ISO 690
References
- ^ ISO Catalogue: Medical devices -- Application of risk management to medical devices
- ^ [http://ec.europa.eu/enterprise/newapproach/standardization/harmstds/reflist/meddevic.html Summary list of titles and references of harmonised standards related to medical devices - DG Enterprise & Industry. European Commission]
External links
- ISO 13485 International Organization for Standardization
- La ISO 14971 en la Red Tecnologías y Productos Sanitarios
