Understanding Corrective and Preventive Action, and Elements of a CAPA System - Webinar by GlobalCompliancePanel

A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer. A system that identifies and eliminates nonconformances and potential nonconformances enables both regulatory compliance and cost savings. This session will discuss the importance, requirements, and elements of a CAPA program, as well as describing the uses of CAPA data. Additionally, the application of risk management to a CAPA program will be reviewed, and a specific risk management system explained. Areas Covered in the Session:

• QSR and ISO 13485 requirements for CAPA
  
• Elements of a cross-procedural CAPA program
  
• Applications of CAPA
  
• CAPA data and its uses
  
• Application of risk management to CAPA program

Who Will Benefit: This webinar will provide valuable assistance to all regulated companies, a CAPA program is a requirement across the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:

• R&D management
  
• Regulatory management
  
• QA management
  
• Consultants
  
• Quality system auditors