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:

Vesna Djordjevic

Date and Time:

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

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From Claims to Compliance: ISO 14060 and the Future of Net Zero

From Claims to Compliance: ISO 14060 and the Future of Net Zero

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Date and Time:

Jul 23 2026 11:00AM Eastern Time (US and Canada)

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Medical Device Cybersecurity: Close the Gap Between Regulatory Requirements and Real-World Implementation

Medical Device Cybersecurity: Close the Gap Between Regulatory Requirements and Real-World Implementation

Speakers:

Date and Time:

Sep 10 2026 11:00AM Eastern Time (US and Canada)

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