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.

The CAPA & Root Cause Investigation Workshop 2016 covers topics such as:

• 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

The CAPA & Root Cause Investigation Workshop 2016 brings together 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