The international standard IEC 62366 medical devices - Application of usability engineering to medical devices is a standard which specifies usability requirements for the development of medical devices. It is harmonized by the European Union (EU) and the United States (US), and therefore can be used as a benchmark to comply with regulatory requirements from both these markets.
Video IEC 62366
Summary of IEC 62366
The IEC 62366 standard calls out the errors caused by inadequate medical device usability have become an increasing cause for concern. IEC 62366 is a process-based standard that aims to help manufacturers of medical devices to design for high usability. It does not apply to clinical decision-making that may be related to the use of the device. The standard will replace ISO/IEC 60601-1-6: Medical electrical equipment - Part 1-6: General requirements for safety - Collateral standard: Usability. Manufacturers of medical electrical equipment who comply with IEC 60601-1-6 need to also comply by extension to IEC 62366 as part of IEC 60601-1 Edition 3.1
Maps IEC 62366
History of IEC 62366
IEC 62366 was published for the first time in 2007. Subsequently in February 2015 it was published the IEC 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices. Subsequently, in May 2016 it was published the IEC/TR 62366-2 Ed 1, Medical devices - Part 2: Guidance on the application of usability engineering to medical devices.
See also
- International Electrotechnical Commission (IEC)
- List of IEC standards
- IEC 60601
References
External links
- "IEC 62366" at International Electrotechnical Commission
Source of article : Wikipedia
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