FMEA has several variants that allow for minimizing risk throughout product development. Design FMEA is a handy means of ...

If you are still using FMEA as your methodology to capture medical device risk management activities, then your risk management process is out of date. And you might be asking why do you need to ...

FMEA is a structured approach used to identify ways in which a product or process can fail, estimate risk associated with specific causes, and prioritize actions that should be taken to reduce risk.

This course presents an overview of the Failure Mode and Effects Analysis (FMEA) approach to calculate risk and proactively avoid potential failures in a process or service. As UB TCIE’s Operational ...

A Failure Mode and Effects Analysis (FMEA) is a “bottom-up” type of system analysis that is required for the standards certification of functional safety: IEC 61508 and all the standards deriving from ...

Participants will learn the purpose and benefits of FMEA, the different types of FMEAs and their focus, QS-9000 FMEA requirements and guidelines, FMEA timing and inputs, and steps required for ...

This asynchronous course presents an overview of the Failure Mode and Effects Analysis (FMEA) approach to calculate risk and proactively avoid potential failures in a process or service. Participants ...