Process Robustness: The New FDA Paradigm 2016

  • 14 Jan 2016
  • Webinar

Description

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

Past Events

Important

Please, check "Process Robustness: The New FDA Paradigm" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Pharma
Science: Life Sciences & Biology

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