| Design More Reliable Medical Devices and Reduce Recalls |
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| Medical
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Studies have shown that 44% of all voluntary medical device recalls are attributable to design errors or deficiencies that may be prevented by adequate design controls. Incorporating an effective risk analysis process can help reduce both design errors and deficiencies in medical devices. Relex Software Corporation can provide a comprehensive risk analysis solution to achieve a risk level as low as reasonably possible (ALARP). Read
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Industry Example
See an example
that demonstrates the use of Relex software modules to meet reliability regulations on a pulse oximeter.
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