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

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

Speakers:

Date and Time:

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

Register
Understanding the Changes to ISO 9001:2026

Understanding the Changes to ISO 9001:2026

Speakers:

Date and Time:

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

Register
Change from prefixes (AS, EN, SJAC, JISQ) to a single IA (International Aerospace) one globally authoritative standard and what's changing

Change from prefixes (AS, EN, SJAC, JISQ) to a single IA (International Aerospace) one globally authoritative standard and what's changing

Speakers:

Date and Time:

Jun 25 2026 11:00AM Eastern Time (US and Canada)

Register