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

Topics

• 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

Who should Attend

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