The Use and Mis-use of FMEA in Medical Device Risk Management 2012 is a webinar that covers topics such as:
- What are the problems with FMEA in risk management?
- How should I use FMEA in performing risk management?
- Is there a role for RPN (Risk Priority Number)?
- How should detectability be used in FMEA?
- Are there FMEA applications in production as well as design?
- Are there other tools to use in conjunction with FMEA?
The Use and Mis-use of FMEA in Medical Device Risk Management 2012 brings together:
- Quality managers responsible for integrating risk management into quality systems
- Product design teams and personnel assigned to use FMEA at medical device companies
- Personnel responsible for verification and validation activities
- Regulatory and compliance personnel who develop premarket filings and technical files for medical devices
- Quality system auditors
