How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment 2016 is a webinar that covers topics such as:
- 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
How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment 2016 is intended for:
- Process engineers
- Formulators
- Quality assurance personnel
- Validation specialists
- Production managers occupied with process and product quality assurance
