Business Knowledge Series course
Presented by Heath Rushing, co-founder and Principal Consultant, Adsurgo LLC
In this free lunch-and-learn webinar, a series of demonstrations will illustrate how to establish a systematic approach to implementing statistical methodologies into a process development and validation program consistent with the 2011 FDA guidance on process validation. These demonstrations are based on the content covered in Statistics for FDA Process Validation Using JMP® Software.
Learn how to
- apply risk management tools prior to DOE studies
- analyze screening and response surface designs
- evaluate scale effects
- characterize inter-batch and intra-batch variability
- employ methods to ensure process control and capability.
Who should attend
Scientists and engineers who need to incorporate statistical concepts into their pharmaceutical process validation quality system
There are no prerequisites for attending this webinar.
This course addresses JMP software.
