Description

This document defines the structured framework for establishing, implementing, and maintaining the Training Management System within a pharmaceutical manufacturing facility. It ensures that all personnel performing activities impacting product quality, safety, and efficacy are adequately trained, qualified, and competent to perform their assigned duties in strict compliance with current Good Manufacturing Practices (cGMP), WHO, FDA, and MHRA guidelines.

The scope encompasses all permanent, temporary, and contract employees working across key departments, including Production, Quality Assurance (QA), Quality Control (QC), Warehouse, Engineering, and Microbiology.