Corrective Actions Preventive Actions - CAPA 101
🎤 Alan M. Golden | 📅 October 22, 2024 | 🕒 11 AM Eastern Time US
  | Description: Corrective Actions/Preventive Actions are an integral part of a robust quality system in both pharmaceutical and medical device manufacturing. The ability to be able to determine the root cause of a product or manufacturing issue and put effective corrections in place is critical to continued product quality. Understanding the process of root cause investigations and the appropriate corrective actions/preventive actions will help ensure continued product quality. CAPA is a required part of both pharma and medical device quality systems. An understanding of the CAPA system and putting into place a robust process will help ensure quality products and smooth manufacturing. |
Areas Covered in the Session :
- Gain an understanding of the CAPA process
- Understand the need for CAPA
- Discuss inputs into the CAPA process
- How to put a good process in place
Who Should Attend:
- Quality Assurance Departments
- Quality Control Departments
- Regulatory Affairs Departments
- Research and Development Departments
- Manufacturing Departments
- Engineering Departments
