The Use and Mis-use of FMEA in Medical Device Risk Management 2012
31 Jul 2012
Webinar
Description
Topics
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?
Who should Attend
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
Past Events
The Use and Mis-use of FMEA in Medical Device Risk Management 2012 - 31 Jul 2012, Webinar (14818)
Important
Please, check "The Use and Mis-use of FMEA in Medical Device Risk Management" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Pharma
