ISO 14971: Difference between revisions
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'''ISO 14971''' is an [[ISO]] standard, published in 2007, that represents the requirements for a risk management system for [[medical device]]s.<ref> |
'''ISO 14971''' is an [[ISO]] standard, published in 2007, that represents the requirements for a risk management system for [[medical device]]s.<ref> |
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[http://www.iso.org/iso/iso_catalogue/catalogue_tc/catalogue_detail.htm?csnumber=38193 ISO Catalogue: Medical devices -- Application of risk management to medical devices]</ref> |
[http://www.iso.org/iso/iso_catalogue/catalogue_tc/catalogue_detail.htm?csnumber=38193 ISO Catalogue: Medical devices -- Application of risk management to medical devices]</ref> |
Revision as of 02:42, 12 April 2010
This article needs additional citations for verification. (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 [citation needed].
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]