
Event Details
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Webinar Dates: January 20β21, 2026
β± Duration: 1 hour
Session Times:
- EMEA: 10:00 AM GMT | 11:00 AM CEST
- Americas: 11:00 AM PST | 2:00 PM EST
- Asia: 8:30 AM IST | 11:00 AM SST | 12:00 PM JST | 2:00 PM AEDT
π Registration Link:
https://www.americanpharmaceuticalreview.com/623033-Speed-Meets-Precision-Fast-Raw-Material-ID-Advanced-Peptide-Characterization/
The rapid expansion of synthetic peptide therapeutics, particularly the growing global demand for GLP-1 receptor agonists, is placing unprecedented pressure on pharmaceutical manufacturing and quality systems. As production scales up, the need for fast, reliable, and non-destructive analytical tools has never been greater.
To address these challenges, Agilent Technologies is hosting a two-part technical webinar that brings together innovative solutions for raw material verification and advanced peptide characterization, helping pharmaceutical manufacturers improve efficiency without compromising quality.
Why This Webinar Matters
Modern peptide drug manufacturing requires analytical workflows that are not only accurate, but also scalable, robust, and time-efficient. Delays in raw material release or limited insight into peptide stability can significantly impact production timelines and product quality.
This webinar showcases two proven analytical approaches designed to streamline workflows while supporting regulatory and quality requirements.
Webinar Highlights
Part 1: Rapid Raw Material Identification β From Pallet to Production, 50% Faster
This session demonstrates how the Agilent Vaya Raman system, powered by patented Spatially Offset Raman Spectroscopy (SORSβ’) technology, enables:
- Fast, non-invasive raw material identification
- Analysis through a wide range of container types
- Significant reductions in material release time
- Improved efficiency in incoming material verification
Attendees will gain insight into how Raman-based identification can accelerate decision-making and reduce bottlenecks in manufacturing operations.
Part 2: Unlocking Peptide Insights β Advanced Stability Assessment with UV-Visible Second-Derivative Spectroscopy
The second session focuses on peptide characterization using the Agilent Cary 3500 UV-Vis Spectrophotometer, highlighting how advanced spectral techniques can:
- Improve resolution and sensitivity using second-derivative spectroscopy
- Enable more accurate monitoring of peptide stability
- Support formulation development and long-term quality control
- Enhance confidence in peptide therapeutic performance
This session is particularly valuable for scientists involved in R&D, analytical development, and quality control.
Who Should Attend
This webinar is ideal for professionals involved in:
- Pharmaceutical manufacturing
- Quality control and quality assurance
- Analytical and formulation R&D
- Regulatory compliance and process optimization
Register Today
Join this informative session to learn how advanced analytical technologies can help you move faster, improve confidence, and maintain precision across peptide manufacturing and characterization workflows.