How to Implement and Maintain a Modern CAPA System while Avoiding Common Pitfalls

This on-demand webinar, hosted by Greenlight Guru, focuses on effectively implementing and maintaining a modern CAPA (Corrective and Preventive Action) system in the medical device industry. During this session you’ll learn best practices for improving CAPA processes and proactive approaches to identify and address potential issues.

Main points covered:
1. Understanding regulatory requirements for CAPA.
2. Common pitfalls in CAPA systems and how to avoid them.
3. How CAPA integrates with other Quality Management System processes.
4. The role of risk management in CAPA.
5. Implementing a proactive approach to CAPA for issue prevention.

Target Audience:
• R&D Engineers and Management
• Regulatory Affairs Professionals and Management
• Quality Professionals and Management
• Medical Device Executives
• Clinical Affairs Professionals and Management

Access the printable slides for this presentation by visiting:
https://www.greenlight.guru/webinar/h...