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In this talk we present an analysis of the new standard ISO 26262 for the automotive industry. We compare this standard to existing regulations of another safetycritical domain, i.e. the medical device industry. As can be expected, a large number of activities coincide, since they simply correspond to common best practices that can also be found e.g. in ISO/IEC 15504. However, some interesting differences can be observed both in philosophy and in wording.

This talk is intended to facilitate communication between the two domains that are driven by the same concern: safety of the end user. We will point out the most striking similarities and differences and translate from one domain to the other.

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