Event
Beginning: 04/09/26
Location: Online
Two sessions are available for this webinar:
- 9 AM BST / 10 AM CEST / 4 PM CST / 5 PM JST
- 4 PM BST / 5 PM CEST / 8 AM PDT / 11 AM EDT
Biotherapeutics require precise structural characterization and stability monitoring throughout development and manufacturing. As biopharma moves toward greater process control and real-time quality assurance, analytical technologies must deliver rapid, information-rich data that support Process Analytical Technology (PAT) strategies.
In this webinar, we will present how Veloci, designed for regulated environments and powered by the innovative A-TEEM™ technology, serves as a powerful PAT-enabling tool for therapeutic protein analysis. Unlike conventional analytical methods that often require multiple techniques and lengthy workflows, Veloci combines absorbance and fluorescence measurements into a single, information-rich dataset, enabling detailed structural assessment, stability monitoring, and early aggregation detection with exceptional sensitivity.
Covered topics: Process analytical technology (PAT) - Critical quality attributes (CQA) - Upstream process control - Downstream analytics - At-line analysis
Key Learning Objectives
By the end of this webinar, participants will be able to:
- Understand key analytical challenges in the structural and stability assessment of therapeutic proteins.
- Appreciate how Veloci enhances structural insight and enables more comprehensive protein characterization compared to conventional techniques.
- Evaluate the benefits of an integrated, single-workflow approach combining absorbance and fluorescence measurements.
- Understand how Veloci supports regulatory compliance, including 21 CFR Part 11 requirements and OPC-UA connectivity for digital laboratory integration.
Who Should Attend:
- Scientists in biopharmaceutical R&D and analytical development seeking advanced structural characterization of therapeutic proteins
- Upstream and Downstream process development professionals seeking advanced analytical tools to support process optimization
- Bioprocess and CMC professionals working on stability studies, comparability, and quality attribute assessment
- PAT specialists and process engineers integrating real-time or at-line analytical technologies
- QC managers and laboratory leaders implementing compliant, digitally integrated analytical workflows in regulated environments
