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How AI can revolutionize FMEA Development

Artificial Intelligence (AI) is already a transformative force in our daily lives.

Publish Date:October 11, 2024

Unlock the potential of ISO 27001 and SCS 9001

Watch the webinar recording to compare the ISO 27001 and SCS 9001 cybersecurity standards.

Publish Date:October 04, 2024

Master the ICT Supply Chain Security Management SCS 9001 Standard: Training Courses for Certification Success

Watch our insightful webinar to explore the comprehensive training courses designed to help you master the SCS 9001 Standard.

Publish Date:July 15, 2024

Conducting IATF 16949 Audits with ASPICE and Functional Safety

Many organizations that are IATF 16949 certified are also implementing Functional Safety, ASPICE, and Product Cyber Security. This is part of the automotive industry’s shift from internal combustion to electric and hybrid engines.

Publish Date:July 10, 2024

Automotive Data Security and Privacy

The amount of software in new automotive vehicle designs continues to escalate, posing a serious threat to automotive data security and privacy, including the privacy of individuals and the complex interactions involved in the driving experience.

Publish Date:July 05, 2024

Net Zero IWA 42 and Carbon Neutrality Standards ISO 14068

This webinar is an informative and exciting discussion on Net Zero Carbon and Carbon Neutrality.

Publish Date:June 21, 2024

Implementing New APQP and Control Plan Using Electronic Workflows

The 3rd Edition New Advanced Product Quality Planning (APQP) manual and 1st Edition Control Plan are in the early rollout phase.

Publish Date:June 07, 2024

Reverse FMEA, A Method to Confirm Risk

RFMEAs are performed after production launch for risk management and detection. They are used to identify critical areas in the process and implement preventive controls to detect failures, aiding in the follow-up to ensure the effectiveness of control plan detection methods.

Publish Date:May 17, 2024

ASPICE 4.0 seen from a Hardware view

The Automotive SPICE® PAM and PRM v4.0 was released on the 29th of November 2023. One notable change is that new process groups were added.

Publish Date:April 26, 2024

Changes to Medical Device Legislation, Adopting ISO 13485 to 21 CFR 820

21 CFR 820 contains the FDA requirements for Quality Management Systems (QMS). These requirements have been established since July 1978.

Publish Date:April 19, 2024