Audience: Application User
Aras Quality Planning uses APQP and FMEA tools to manage risk, improve quality and achieve compliance across a broad range of industry standards. Aras Quality Systems uses CAPA and RCA capabilities to capture quality issues, thoroughly analyze and drive product & process changes to eliminate future re-occurrence.
In this hands-on session, you will learn how to incorporate quality design considerations throughout the entire product lifecycle by utilizing a closed-loop quality system to incorporate feedback from in-use products to improve the quality of future designs. You will learn to create a Corrective Action Plan with relationships to:
- Quality Events: Audit Findings, NCR, & PR
- Containment: Purge, Hold, & Stop Ship Notices
- Analysis: Root Cause
- Corrective Actions: Deviation, Rework Orders, & Waivers
- Preventive Actions: DFMEA & PFMEA