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Process Robustness: The New FDA Paradigm 2016
14 Jan 2016
Webinar
Home
Process Robustness: The New FDA Paradigm 2016
Key Topics
Define common terms
Key concepts associated with process robustness
Tools and metrics
Detail a methodical approach to robust process development
Who should Attend
QA Specialists (Senior Level)
Sr. Directors/Directors
Quality System Consultants
Compliance Professionals
Technical Services Managers
Production Management
Process Engineers
Read more
Past Events
Process Robustness: The New FDA Paradigm 2016 - 14 Jan 2016, Webinar
(55531)
Process Robustness: The New FDA Paradigm 2026
Important
Please, check "Process Robustness: The New FDA Paradigm" official website for possible changes, before making any traveling arrangements
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