Overview
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Explore how Biacore™ SPR technology supports pharmaceutical development from discovery through quality control in this comprehensive webinar. Learn about real-time, label-free detection capabilities and unmatched sensitivity that make SPR a trusted method in European, Japanese, and US pharmacopoeia for potency assays, comparability studies, and kinetic characterization. Discover the next generation Biacore™ SPR system's capabilities for assay transfer from legacy platforms through a customer success story demonstrating the seamless transition of a validated Biacore™ SPR T200 assay to the Biacore 1S+ platform. Understand how SPR supports robust method validation under ICH guidelines and characterizes activity and potency for therapeutic performance. Gain insights into validation excellence covering key parameters including accuracy, precision, specificity, robustness, and limit of quantification aligned with GMP standards. Examine practical tools and strategies for implementing Biacore™ SPR systems as a cornerstone of quality control workflows while maintaining compliance with global pharmacopeial standards and future-proofing analytical methods for evolving pharmaceutical technologies.
Syllabus
Biacore™ SPR in QC Confident, compliant, and future ready A success story in seamless assay transf
Taught by
Labroots