Using DFMEA/PFMEAs for Risk Management in Medical Device Manufacturing

by Michael B. Checketts published on October 15, 2020

This webinar will take a perceived complex issue and present ways and means of performing D-FMEA & P-FMEA simply and effectively. Once established for any particular design or process the same FMEA can be reviewed again each time an update is desired or required throughout the life cycle of the product / process.

Understanding the relationship between UNECE WP.29 R155 and ISO/SAE 21434

Understanding the relationship between UNECE WP.29 R155 and ISO/SAE 21434

Speakers:

Vignesh Sambandan

Date and Time:

Jul 31 2024 11:00AM EST

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