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.

Corrective and Preventive Action (CAPA) per FDA Requirements 2018 covers topics such as:

• CAPA Concepts
• What is CAPA?
• CAPA Procedure

Corrective and Preventive Action (CAPA) per FDA Requirements 2018 is intended for attendees from:

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

CAPA is a concept within Good Manufacturing Practice (GMP)