Hardly any other industry is more strictly regulated than medical technology. Medical devices must first undergo lengthy approval processes before they can be used in practice. One could say that innovation is subject to severe delays due to partly outdated processes.
By developing a pilot solution that will form the basis for international standardization, an attempt is being made to speed up medical technology software certification enormously. Special AI software tools should enable complex specifications to be easily checked for completeness, consistency and logic in the future, thus ensuring greater transparency and security in the certification process of programmable electronic medical systems.
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