Corrective and Preventive Action (CAPA) in Medicinal Products Manufacture
Instructor
Syed Salman
Reviews
Course Overview
A company’s Corrective and Preventive Action (CAPA ) system establishes how personnel should deal with manufacturing problems that have occurred or that may occur if not prevented. This module explains the principles of corrective and preventive action and describes typical CAPA procedure. It goes on to introduce root cause analysis and outline the role of progress tracking, escalating, and trending of CAPA procedures.
Learning Objectives
• Explain what a CAPA system is and describe how it operates in a company’s Quality Management System
• Describe how a typical CAPA procedure is carried out
• Outline the purpose and practice of root cause analysis
• Discuss the role of progress tracking, escalating, and trending of CAPA procedures
What You'll Learn?
- This module provides essential training for all personnel who work in a manufacturing environment in the pharma/biotech industry.