Webinar 2:
Particle-Size Analysis Through Closed Containers
20 October 2026
Using the NanoLabSizer in Pharmaceutical Formulation Development and QC
20 October 2026 | Two live sessions | Expert presentation and live Q&A
Opening a container, transferring material or diluting a sample can influence both the sample and the analytical workflow. But can particle size be measured without opening the container?
In this webinar, we will explore how particle size can be measured directly through closed, transparent containers using the NanoLabSizer.
We will discuss how this non-destructive approach can support pharmaceutical formulation development, stability studies and routine offline measurements while reducing sample handling.
The NanoLabSizer can measure through containers such as vials, tubes, syringes, flasks and IV bags, without opening, transferring or diluting the sample.
Measure without opening the sample
One sample. Less handling.
Closed-container particle-size analysis can support:
- Formulation development
- Stability studies
- Routine offline measurements
- Pharmaceutical quality control
- Reduced sample handling
Using the NanoLabSizer, this webinar shows how particle size can be measured directly through:
- Vials
- Tubes
- Syringes
- Flasks IV
- bags
- Other transparent bioprocess containers
No opening. No sample transfer. No dilution.
The sample remains protected, making the approach particularly relevant for sensitive, valuable or sterile formulations.
New to the NanoLabSizer?
Learn how the NanoLabSizer enables non-destructive particle-size measurements directly through closed, transparent containers.
What will you learn?
During this webinar, we will discuss:
- How particle size can be measured through closed, transparent containers
- How the NanoLabSizer reduces the need for opening, transfer and dilution
- Which containers and sample types can be suitable for closed-container analysis How the approach can support formulation development and stability studies
- Where non-destructive measurements can fit into routine pharmaceutical analysis and QC
- How repeated measurements can be performed while keeping the sample protected
- What to consider when selecting a measurement configuration for your application
Who should attend?
This webinar is relevant for professionals working with pharmaceutical, biopharmaceutical and nanoparticle formulations, including:
- Formulation scientists
- Analytical scientists
- Pharmaceutical development scientists
- Quality control professionals
- Stability-study teams
- LNP and liposome researchers
- Biopharmaceutical scientists
- Laboratory managers
- R&D managers
- Scientists working with sensitive, sterile or limited-volume samples
- Scientific and technical decision-makers
Meet the speaker
Carl Schuurmans, Associate director Applied PAT – InProcess-LSP
Carl Schuurmans is Associate Director at InProcess-LSP, where he leads the Applied Process Analytical Technologies group.
He previously held research positions at Philips Research, Utrecht University and Harvard University.
His work focuses on pharmaceutical technology and process analytics, with particular emphasis on in-process particle-size measurement using Spatially Resolved Dynamic Light Scattering (SR-DLS).