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 : Overview of California SB 253 and 261

Speakers:

Date and Time:

Feb 3 2026 11:00AM Pacific Time (US and Canada)

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Upcoming Webinar : Transitioning to PAM 4.0: For OEMs and Suppliers

Speakers:

Date and Time:

Jan 27 2026 11:00AM Eastern Time (US and Canada)

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