How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment 2016

Topics

• Code of Federal Regulations Title 21
• Data-driven fault diagnosis and process monitoring methods
• Pharmaceutical industry basic unit operations
• Monitoring and control of process parameters and component and device characteristics during production
• Process and endpoint monitoring and control tools
• Quality by Design (QbD) and modern process monitoring systems
• Current GMP practices and risk-based PAT framework

Who should Attend

• Process engineers
• Formulators
• Quality assurance personnel
• Validation specialists
• Production managers occupied with process and product quality assurance