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5th Annual Forced Degradation Strategies for Small Molecules

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

Main Conference Day Two

Main Conference Day Two

Wednesday, February 27th, 2008

8:00Morning Coffee
8:30

Chair's Remarks and Recap of Day One

Eric Nelson, PhD, Group Leader, JOHNSON & JOHNSON

Alex Opio, PhD, Scientist, PFIZER, INC.

8:45

Leverage Forced Degradation Testing To Improve Stability Prediction and Reduce Time to Market

Stephen R. Byrn, PhD, Professor and Head, Department of Industrial and Physical Pharmacy, PURDUE UNIVERSITY

9:15

Accelerated Stability Assessment Program (ASAP): Using Science to Set Shelf Life

Ken Waterman, PhD, Research Fellow, PFIZER, INC.

9:45

Leverage Forced Degradation Case Studies That Facilitate Drug Discovery and Development Decision-Making

Jay Xu, PhD, Senior Scientist, Structural Chemistry, ARENA PHARMACEUTICALS, INC.

10:1530 Minute Networking & Refreshment Break
10:45

Development and Use of Orthogonal Methods to Analyze Drug Substance and Drug Product Pharmaceutical Degradants

Fengmei Zheng, PhD, Sr. Scientist, JOHNSON & JOHNSON, PHARMACEUTICAL RESEARCH & DEVELOPMENT

11:15

Use of Mixed-Mode Ion-Exchange Solid Phase Extraction To Characterize Pharmaceutical Drug Degradation

Margaret Landis PhD, Senior Principal Scientist, PFIZER, INC.

11:45

Orthogonal Methods and Characterization Technologies To Characterize Degradants and Impurities

Panelists:
Ivelisse Colon-Rivera, PhD, Sr. Principle Scientist, PFIZER, INC.

Margaret Landis, PhD, Principal Scientist, Research Formulations Group, PFIZER, INC.

Fengmei Zheng, PhD, Sr. Scientist, JOHNSON & JOHNSON, PHARMACEUTICAL RESEARCH & DEVELOPMENT

If you are interested in participating in this panel, please contact Mike Vidoni at 212 661-3500, ext.3197, mvidoni@iirusa.com for more information

12:15Luncheon
1:15

Strengthen Forced Degradation Efficiencies by Implementing New High Throughput and Automated Technologies

Dinos Santafianos, PhD, Principal Scientist, PFIZER, INC.

1:45

Automated Methods Development: The New Paradigm

Rosario LoBrutto, PhD, Group Head, Pharmaceutical and Analytical Development, NOVARTIS Pharmaceuticals Corporation, Co-Editor/Author HPLC for PHARMACEUTICAL SCIENTISTS (Published by Wiley)

2:15

Biomolecule Perspective: Photostability of a Monoclonal Antibody

Melissa Perkins, PhD, Director of Drug Product Development, Pharmaceutical Sciences, HUMAN GENOME SCIENCES

2:45

Global Harmonization of Forced Degradation Studies

Fenghe Qiu, PhD, Principal Scientist, Analytical Sciences, BOEHRINGER INGELHEIM

3:15Interactive Q&A Panel with the Speakers
4:00

Conference Concludes



Event Sponsors

  • Atlas Material Testing Technology

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