Join this webinar to explore how modern Raman spectroscopy is transforming biopharma fill-finish quality control through faster analysis, multi-attribute insight, and scalable model transfer.
Raman spectroscopy offers real advantages for biopharma fill-finish QC — non-destructive measurement, minimal sample prep, through-container analysis, and the ability to support multi-attribute testing in a single run.
But deploying it reliably across instruments and sites is where most implementations run into trouble. This webinar addresses that directly: how to build chemometric models that transfer, manage fluorescence interference, and integrate Raman workflows into broader Industry 4.0 data environments.
As fill-finish operations scale - more products, more sites, more instruments - maintaining consistency in Raman-based QC becomes increasingly complex. Model revalidation across instruments is time-consuming. Fluorescence interference complicates measurements. And integrating spectroscopic data into GMP-compliant data systems adds another layer of overhead.
This session covers practical strategies for tackling fill-finish with scalable model transfer, helping you to achieve better outcomes in the real world.
In this session you will:
- See how multi-attribute Raman measurements can replace multiple separate assays in fill-finish workflows
- Get practical guidance on sampling through glass and managing fluorescence interference
- Understand the chemometric and operational requirements for transferring models across instruments and sites
- Hear how Industry 4.0 connectivity is being used to embed Raman QC into real-time release and batch disposition workflows.
Interested? Register now!
Sudhir Dahal - Product Manager, Thermo Fisher
Sudhir Dahal is the Product Manager for Research Raman Products at Thermo Fisher Scientific, where he focuses on bringing advanced Raman spectroscopy solutions to market for demanding pharmaceutical and industrial applications.
With over a decade of experience in analytical instrumentation, Sudhir works closely with customers, application teams and R&D to translate real-world QC challenges – such as biopharma fill-finish testing, data robustness and scalability – into practical, automation-ready solutions.
He holds a Ph.D. from the University of Maryland, Baltimore County, where he developed spectroscopy-based methods for biomedical analysis. Sudhir is passionate about connecting technology, workflow, and market needs to enable smarter, data-driven quality control.
Is the panel discussion free?
Yes – there is no charge to watch the panel discussion, either live or on-demand.
When will the panel discussion take place?
15 April 2026 at 4PM GMT.
Can I watch it later?
The panel discussion will become available to watch on-demand shortly after the live webinar takes place.
What are the benefits of attending live?
You’ll be able to ask the speakers your questions, which will be answered live in the Q&A towards the end of the session.
How long will the panel discussion be?
This panel discussion will last up to an hour.
What do I need to watch this panel discussion?
All you need is a computer with an internet connection. We recommend using headphones if possible if you’re in an office environment.
