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 integrate Quality by Design principles in a pharmaceutical quality system.

Learn how to

• Set meaningful specifications.
• Evaluate information from assay validations.
• Analyze screening and response surface designs.
• Link information from pharmaceutical development studies to a process control plan.

Who should attend

Scientists and engineers who need to integrate Quality-by-Design (QbD) principles into their pharmaceutical development and quality systems

Formats available	Standard Duration (duration can vary, see event schedule for details)
Live Web Classroom:	1-hour session	System Requirements

There are no prerequisites for attending this webinar.

This course addresses JMP software.

Data Intervals

MSA for Assays

Establish Purpose for QbD Studies and CQAs

Identify Potential Factors Using Ishikawa

Prioritizing Factors Using FMEA

D-Optimal Design

Augmenting a D-Optimal Design: I-Optimal Design

Determining Critical Process Factors for the Control Plan

Process Control

Process Capability