Among other key topics, this training program will focus on what can be monitored in mixing operations, wet granulation operations, dry granulation operations, compaction operations, and coating operations.
Why Should You Attend:
This webinar will provide an insight into the practical aspects of the process monitoring technology and will be an invaluable source of information on various methods and approaches that will allow you to optimize solid dosage processes in both R&D and production. Attendees will learn about regulatory guidance and requirements designed to improve real-time process monitoring and control, as well as technical aspects of various instrumentation techniques.Learning Objectives:
- What can be monitored in mixing operations
- What can be monitored in wet granulation operations
- What can be monitored in dry granulation operations
- What can be monitored in compaction operations
- What can be monitored in coating operations
- PAT guidance and process monitoring devices
- Monitoring for real-time quality management
- FDA guidance and methodologies for risk-based monitoring
Areas Covered in the Webinar:
- Data-driven fault diagnosis and process monitoring methods
- Code of Federal Regulations Title 21
- Monitoring and control of process parameters and component and device characteristics during production
- Pharmaceutical industry basic unit operations
- Quality by Design (QbD) and modern process monitoring systems
- Process and endpoint monitoring and control tools
- Current GMP practices and risk-based PAT framework
Who Will Benefit:
- Formulators
- Process engineers
- Validation specialists
- Quality assurance personnel
- Production managers occupied with process and product quality assurance
Course Provider
Michael Levin,
