Quality by Design 2015 - Quality by Design: Establishing a Systematic Approach to Pharmaceutical Development
Date2015-06-08
Deadline2015-06-07
VenueOnline event, USA - United States
KeywordsPharmaceutical Development; Quality by Design; Risk management training
Websitehttps://bit.ly/1Hqybah
Topics/Call fo Papers
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
support-AT-compliance4all.com
www.compliance4all.com
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
support-AT-compliance4all.com
www.compliance4all.com
Other CFPs
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- How to Respond to an FDA Investigation: What happens when the FDA threatens to shut you
- Supplier Quality Management - Implement it Now or Pay for it Later
- Using the ISP98 Model Forms for Standby Letters of Credit
- THEIIER-7th International Conference on Recent Advances in Medical Science (ICRAMS-2015)
Last modified: 2015-04-15 18:50:50