The document outlines various components of a Quality Management System (QMS), including management responsibility, resource provision, and product realization processes. It emphasizes the importance of documentation control, customer satisfaction, and compliance with internal audits. Additionally, it addresses topics such as training, infrastructure, and the control of non-conforming products.

1. 850 – Improvement
421 – Maintain Document Awareness
423 – QMS Document Control
Customers Customers
500 – QMS - Management
Responsibility
610 – Provision of QMS
Resources
620 – Skills & Training
630 – Production Facility
Infrastructure
640 – Work Environment
Resource Management
710 – Planning of Product Realization
740 - Purchasing
751 - Control of Production Systems
751DPD – Digital Product Definition QA Plan
753 – Identification & Traceability
754 – Customer Property
755 – Preservation of Product
760 – Control of Monitoring & Measuring Equipment
Product Realization
421PMA - PMA Fabrication Inspection System
823 – Process Compliance
824 – Product Conformance
830 – Non-Conforming Product Control
830 MRB Plan - Materials Review Board Plan
840 – QMS Performance Analysis
Measurement, Analysis & Improvement
Continual Improvement of the Quality Management System
424 – Control of Records
430 – Configuration Management
822 – Internal Audit
Management Responsibility
Input Output
Requirements
720 – Customer
Related
Processes
821 – Customer
Satisfaction
Satisfaction
Product