Pharmaceutical Quality Systems – 2018 Workshop

Topics

• Regulatory Requirements
• Pharmaceutical Quality Systems in GMP
• Effective Handling of Deviations
• PQS Elements
• Laboratory PQS Compliance
• Change Control Management
• Root Cause Analysis and CAPA Investigations
• Failure Investigations
• Handling Complaints and Recalls
• Annual Product Quality Review
• Quality Metrics
• Quality Risk Management
• Case Studies and Practical Sessions

Who should Attend

• Quality Control Departments
• Quality Assurance Departments
• Manufacturing Departments
• Production Departments
• Regulatory Affairs Departments
• Operations Departments
• Documentation Departments
• Engineering Departments
• Warehousing Departments
• Facilities Departments
• Laboratory Staff