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.

Upcoming Webinar : Updates on IATF 16949, IA 9100, ISO 13485, and ISO 23485

Upcoming Webinar : Updates on IATF 16949, IA 9100, ISO 13485, and ISO 23485

Speakers:

Chad Kymal, Frankie Breedlove, William kovacich

Date and Time:

Oct 28 2025 11:00AM Eastern Time (US and Canada)

Register