ISO 62304 – Software Life Cycle Processes, the Challenges for Medical Devices

by Pete Sparacio published on November 14, 2023

Following an introduction of the company (Ametek/Rauland) and its products, the presentation provides a brief description of the journey Rauland, a medical device company and a leader in healthcare and education communication systems, is on to continue to strengthen its level of compliance with ISO-62304.

Watch the recording to know more..

 

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)

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

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
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:

Stephen Hall

Date and Time:

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

Register
Related Training
Cybersecurity for Medical Devices
Internal Auditor Training Based on the International MDSAP Audit Approach
Understanding ISO 14971:2019 Application of Risk Management to Medical Devices
ISO 14971 Application of Risk Management to Medical Devices - PFMEA Overview
ISO 14971:2019 Application of Risk Management to Medical Devices Including DFMEA and PFMEA