Corrective and Preventive Action (CAPA) per FDA Requirements 2018

Corrective and Preventive Action (CAPA) per FDA Requirements 2018 is a webinar that provides knowledge on how FDA investigates CAPA in organizations, and be prepared for an audit in your organization.

Topics

• CAPA Concepts
• What is CAPA?
• CAPA Procedure

Who should Attend

Attendees from:

• Documentation Managers
• Quality Assurance
• Document Control
• Records Managers
• Medical Affairs
• Compliance
• IT

CAPA is a concept within Good Manufacturing Practice (GMP)