Failure Mode and Effects Analysis for Design Improvement and Design Control 2015
05 Aug 2015
Webinar
Key Topics
The wrong practices in FMEA
FMEA procedure-the right way
New paradigms for design improvement
Using FMEA to improve the design
Using FMEA for verifying design outputs
Using FMEA for design inputs
Identifying critical design features
Avoiding wrong practices FMEA practices for efficient results
FMEA for planning design validation
Using best strategies to mitigate risks
Who should Attend
Quality assurance supervisors
Senior managers
R&D engineers
Design engineers
Quality professionals
Production supervisors
Compliance professionals
Regulatory professionals
Production engineers
Manufacturing engineers
Document control specialists
Quality auditors
Past Events
Failure Mode and Effects Analysis for Design Improvement and Design Control 2015 - 05 Aug 2015, Webinar (17480)
Failure Mode and Effects Analysis for Design Improvement and Design Control 2026
Important
Please, check "Failure Mode and Effects Analysis for Design Improvement and Design Control" official website for possible changes, before making any traveling arrangements
Event Categories
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Pharma
