Event Registration (EVENT: 673365

Meeting Regulatory and Technical Requirements for Organic Impurity Analysis
Tuesday, September 24, 2013 at 11:00 AM EDT for the US and Tuesday, October 1, 2013 at 15:00 PM CET for Europe
Organic impurities cover a wide spectrum of compounds that have varying structures, behaviors, and characteristics. Organic impurities can result from manufacturing, storage conditions, or degradation resulting from light, heat, and other external factors. Deciding what technology or analytical methods to use to detect and measure organic impurities is a challenge. This 60-minute webcast will provide insight on regulatory, compendial, and ICH requirements on organic impurity control and analysis. Learn from leading experts on best practices in analytical method development, method selection, and method validation for detecting and quantifying organic impurities in drug substances and drug products. Key Learning Objectives • Learn from experts on the latest regulatory and compendial requirements for organic impurity control and analysis in drug substances and drug products • Gain insight on selecting the appropriate analytical methods for detection, analysis, and quantification of organic impurities • Learn from case studies on how best to ensure product quality
Moderator: Patricia Van Arnum Executive Editor Pharmaceutical Technology Speakers: Tim Watson, PhD Research Fellow GCMC Advisory Office Pfizer Mark Argentine, PhD Senior Research Advisor Analytical Sciences R&D Eli Lilly Hildegard Brümmer, PhD Operational Laboratory Manager SGS Life Science Services, Berlin
IMPORTANT - PLEASE READ This is a FREE streaming audio Webcast and does not require a phone line. If you have any questions regarding this Webcast, please contact Sara Barschdorf, sbarschdorf@advanstar.com. Register for this FREE Webcast!
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