The ISO 12971 standard on risk management for medical devices describes risk analysis tools such as PHA, FTA, FMEA, HAZOP, and HACCP but does not provide the depth needed to use the tools correctly. These tools are therefore often misused or used incorrectly, or not used at all. That is why there are almost 900 device recalls a year. This webinar will take you to the depth needed with best practice examples from medical device and other industries.