CAPA & Root Cause Investigation Workshop 2016

The CAPA & Root Cause Investigation Workshop 2016 is dedicated to identifying non-compliance, understanding the root cause, and responding with appropriate corrective and preventive actions for the Pharmaceutical companies.

Key Topics

• Verifying root cause, Corrective Actions/ Preventive Action Plan
• Key strategies in responding to FDA’s 483
• Correction, Corrective Action, or preventive Action?
• Strategies of Implementing an Effective CAPA system
• CAPA: Principles, System, Implementation and Process improvements and the use of Risk Management Techniques

Who should Attend

Pharmaceutical directors, heads, vice president, presidents, senior managers, proprietors, general managers and managers from product manufacturers producing API and formulations with responsibilities in:

• Quality Control
• Quality Assurance
• Production
• Manufacturing
• Engineering