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DRUG DISCOVERY & DEVELOPMENT Presents an Educational, Streaming Audio Webcast Removing Roadblocks to Chromatographic Method Development and ValidationAre trial-and-error practices slowing down your chromatographic methods development processes?CLICK HERE TO REGISTER TODAY! Validating pharmaceutical chromatographic methods are time-consuming, error-prone processes. And, they are riddled with compliance concerns. As a result, laboratory productivity decreases while both the time and costs associated with bringing products to market increases. Science-driven organizations are challenged to better exploit key results to increase efficiency and deliver answers faster, without compromising data quality or increasing costs. Through this webcast, you can gain insight into the trials and tribulations of chromatographic method development and validation for drug discovery and development applications. Participants will learn:
• What bottlenecks do empirical methods development approaches create?
• How can the methods development and validation processes be streamlined?
• How can informatics solutions facilitate methods development?
• How can you successfully convert from an empirical- to informatics-based approach? Don’t miss this informative webcast designed to help you better manage your methods development, validation, and compliance processes. Speakers
James Netterwald, PhD, MT (ASCP)
Senior Editor
DRUG DISCOVERY & DEVELOPMENT
• Hear about the current practices that researchers use to develop and validate methods through empirical processes, including the challenges they face. Lauren Wood
Informatics Product Manager
Waters Corporation
• Learn how informatics solutions can help streamline the workflow challenges while improving productivity, reducing operational costs, and accelerating product commercialization.
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