Statistical Concepts of Process Validation 2017

  • 05 Jul 2017
  • Webinar

Description

Topics
  • Explain the FDA’s approach as documented in Warning Letters
  • Understand the QSR requirements for process validation
  • State the statistical model that links process input and process output
  • Understand the ISO 13485 requirements for process validation
  • Understand the role of process capability and describe the desired values of the indices
  • Link sampling verification to the process model
  • Describe the role of challenge points in Operational Qualification
  • Understand the role of designed experiments in determining the input parameter space
  • Recognize the role of process validation in Risk Management
Who should Attend
  • Quality Engineers
  • Quality Managers
  • Production Supervisors
  • Production Managers
  • Production Engineers
  • Manufacturing Engineers
  • Process Owners
  • Design Engineers

Past Events

Important

Please, check "Statistical Concepts of Process Validation" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Health & Medicine: Medical device, Pharma
Technology: Biotechnology

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