How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment 2016
07 Jan 2016
Webinar
Key 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
Past Events
How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment 2016 - 07 Jan 2016, Webinar (55893)
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Important
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