Articles by Stephen Colgan - Pharmaceutical Technology

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Articles by Stephen Colgan

Stephen Colgan


Articles
Using Quality by Design to Develop Robust Chromatographic Methods
September 2, 2014

The quality-by-design principles used to control process variability are equally important to measurement systems because process variability includes contributions from measurement system variability. The authors use real-life examples from drug development projects to outline how an understanding of chromatographic measurement system variability might be achieved.

Pharmaceutical Stability: Scientific and Regulatory Considerations for Global Drug Development and Commercialization
November 3, 2012

A two-day workshop on the "science behind pharmaceutical stability" was held in conjunction with the Annual Meeting of American Association of Pharmaceutical Scientists (AAPS) on Oct. 21-22, 2011 in Washington, DC.

AAPS Workshop Summary
November 2, 2012

A two-day workshop on the "science behind pharmaceutical stability" was held in conjunction with the Annual Meeting of American Association of Pharmaceutical Scientists (AAPS) on Oct. 21-22, 2011 in Washington, DC.

Early Development GMPs for Stability (Part IV)
September 2, 2012

IQ Consortium representatives explore and define common industry approaches and practices for applying GMPs in early development, with a focus on stability.

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