This document outlines the components of a six system quality inspection model for pharmaceutical manufacturing. It describes the six systems that should be included in a quality system: quality system, production system, facility and equipment system, laboratory control system, material control system, and packaging and labeling system. For each system, it lists the key aspects that should be inspected to ensure compliance with cGMP regulations. The goal is for this model to help manufacturers comply with cGMP requirements and implement an effective quality system.