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