Developing an Effective CAPA Program for GMP Operations 2015

Topics

• Roles and responsibilities of manufacturers
• Hy an effective CAPA system is important
• Determining root causes
• Identifying sources of infractions
• CAPA Tracking System and documentation

Who should Attend

• Quality Assurance scientists
• Laboratory Analysts
• QA/QC Managers
• QA/QC Analysts
• Inspectors
• Auditors
• Manufacturers of raw materials and excipients
• Pharmaceutical development and manufacturing personnel
• Contract laboratory Organization personnel