Design of Experiments (DOE) for Process Development and Validation 2017

  • 28-29 Sep 2017
  • DoubleTree by Hilton Las Vegas Airport, NV, United States

Description

Design of Experiments (DOE) for Process Development and Validation 2017 is a seminar that covers topics such as:

  • Utilize risk management tools to identify and prioritize potential critical process parameters
  • Identify critical quality attributes (CQAs) that will be used as responses in your designs
  • Be able to design and analyze screening designs including a factorial, fractional factorial, and D-optimal design
  • Identify critical process parameters and develop a functional relationship between those process parameters and your critical-to-quality attributes (CQAs) using both screening and response surface designs
  • Be able to design and analyze response surface designs including central composite designs (CCDs), Box-Behnken designs, and I-optimal designs
  • Understand the need for adding center points to a design
  • Use systematic understanding from DOE studies to update the control plan that is part of the overall risk management plan
  • Present results of DOE studies

Design of Experiments (DOE) for Process Development and Validation 2017 brings together pharmaceutical, biopharmaceutical, and medical device professionals involved in product and/or process design:

  • Design Engineer
  • Process Scientist/Engineer
  • Regulatory/Compliance Professional
  • Product Development Engineer
  • Six Sigma Green Belt
  • Design Controls Engineer
  • Continuous Improvement Manager
  • Six Sigma Black Belt

Past Events

Important

Please, check "Design of Experiments (DOE) for Process Development and Validation" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Pharma

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