Quality by Design: Establishing a Systematic Approach to Pharmaceutical Development

June 8, 2015· Ended
Conference
Fremont, United States
In Person

About This Event

Overview:
This webinar focuses on how to establish a systematic approach to pharmaceutical development that is defined by Quality-by-Design (QbD) principles. In addition, this webinar teaches the application of statistics for setting specifications, assessing measurement systems, developing a control plan as part of a risk management strategy, and ensuring process control/capability. All concepts are taught within the product quality system framework defined by requirements in regulatory guidance documents.

Learn How to:

Implement QbD principles from discovery through product discontinuation
Apply statistics to set specifications and validate measurement systems
Utilize risk management tools to identify and prioritize potential critical process parameters
Establish your design space
Develop a control plan as part of a risk management strategy
Ensure your process is in (statistical) control and capable.

Compliance4All
Adam Fleaming
Phone: +1-800-447-9407
Event Link: http://bit.ly/1Hqybah
[email protected]
www.compliance4all.com

Event ID: e5ga6tq
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