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Home»Events»5th Annual Forced Degradation...Conference Documentation

5th Annual Forced Degradation Strategies for Small Molecules

February 25 - 27, 2008 | Sheraton Inner Harbor Hotel, Baltimore, MD

Conference Documentation

Conference Documentation

This page will be used to provide paid delegates of the conference with access to any presentations that were not included in the conference documentation. Only paid conference delegates have permission to access IIR online documentation.

While these presentations were not available to be included in your conference documentation, IIR is pleased to make them available to all conference delegates through this web site.

You will need the freely available Adobe Acrobat Reader, which is available by clicking here


Tuesday, February 26, 2008 

Kick-Start the Evolution of Stability Indicating Methods with Forced Degradation
8:45 am
Eric Nelson, PhD, Group Leader, Johnson & Johnson

Apply Forced Degradation of Polyunsaturated Fatty Acids under Free Radical Conditions as a Model to Mimic Their Metabolism in vivo: Mechanism, Analysis, And Biological Significance
10:45 am
Huiyong Yin, PhD, Research Assistant Professor, Vanderbilt University School Of Medicine

Understanding Genotoxic Degradation: Impact on Science and Compliance Strategies
1:45 pm
J. Derek Jackson, Scientist, Transform Pharmaceuticals, Inc.

Trace Analysis of Impurities with Potential Genotoxicity in Pharmaceutical Samples
2:15 pm
Ivelisse Colon-Rivera, PhD, Sr. Principle Scientist, Pfizer, Inc.


Wednesday, February 27, 2008 

Development and Use of Orthogonal Methods to Analyze Drug Substance and Drug Product Pharmaceutical Degradants
10:45 am
Fengmei Zheng, PhD, Sr. Scientist, Johnson & Johnson, Pharmaceutical Research & Development

Automated Methods Development: The New Paradigm
1:45 pm
Rosario LoBrutto, PhD, Group Head, Pharmaceutical and Analytical Development, Novartis Pharmaceuticals Corporation, Co-Editor/Author HPLC for Pharmaceutical Scientists (Published by Wiley)

Biomolecule Perspective: Photostability of a Monoclonal Antibody
2:15 pm
Melissa Perkins, PhD, Director of Drug Product Development, Pharmaceutical Sciences, Human Genome Sciences

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