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.

Automotive SPICE Updates: Key Changes in the upcoming PAM 4.1 and ASPICE Guidelines 3rd Edition

Speakers:

Vesna Djordjevic

Date and Time:

Jul 9 2026 11:00AM Eastern Time (US and Canada)

Register

ISO 14001:2026 Explained: Key Changes and Transition Requirements - What Organizations Need to Know

Speakers:

Chad Kymal, William Kovacich

Date and Time:

Jun 16 2026 11:00AM Eastern Time (US and Canada)

Register