Are trial-and-error practices slowing down your chromatographic methods development processes?
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 free webcast, you can gain insight into the trials and tribulations of chromatographic method development and validation for drug discovery and development applications.
James Netterwald, PhD, MT (ASCP)
DRUG DISCOVERY & DEVELOPMENT
• Hear about the current practices that researchers use to develop and validate methods through empirical processes, including the challenges they face.
Informatics Product Manager
Filed Under: Drug Discovery