Date: October 16, 2025
Time: 8:00 AM (PT), 11:00 AM (ET), 5:00 PM (CET)
Are you looking to gain more confidence in your analytical methods? Wondering how to future-proof your QC workflows while staying aligned with global pharmacopeial standards?
Join us for a session on how Biacore™ SPR technology supports pharmaceutical development, from discovery to quality control. With real-time, label-free detection and unmatched sensitivity, Biacore SPR technology is a trusted method in European, Japanese, and US pharmacopoeia for use in potency assays, comparability studies, and kinetic characterization.
Discover how the next generation Biacore™ SPR system enables assay transfer from legacy platforms. Listen to one of our customers sharing their experience in successfully transferring a validated Biacore™ SPR T200 assay to the Biacore 1S+ platform.
This webinar is designed for those in need of reliable, validated methods that scale with evolving technologies. We’ll walk through how SPR supports robust method validation under ICH guidelines and how it characterizes activity and potency for therapeutic performance.
This session provides you with practical tools and insights to make Biacore™ SPR system a cornerstone of your QC strategy.
Learning Objectives
- Explore how Biacore™ SPR system is used in pharma QC.
- Validation excellence: Key parameters - accuracy, precision, specificity, robustness, and LOQ—aligned with GMP standards.
- Seamless transfer: Demonstrated success in transferring the method from T200 to 1S+, with comparable outcomes post-optimization.
Webinars will be available for unlimited on-demand viewing after live event.