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.

ISO 14001 está cambiando: ¿Tu sistema está listo?

Speakers:

Date and Time:

May 7 2026 10:00AM Mexico City

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Digitalization of Product Development and the Shopfloor

Speakers:

Antony John, Chad Kymal

Date and Time:

Apr 30 2026 11:00AM Eastern Time (US and Canada)

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