Webináře Thermo Fisher Scientific duben a květen 2026
Imaging and top-down analysis of intact protein complexes in tissue
Date: Thursday, April 16, 2026
Time: 11:00 AM British Summer Time
Duration: 45 minutes
Native ambient mass spectrometry (NAMS) enables the study of proteins and their complexes directly in tissue. The latest developments in NAMS will be presented, including innovative MS imaging and on-tissue native top-down MS workflows.
Topics will include:
- Analysis of membrane proteins
- Identification of protein-metal complexes implicated in neurodegenerative disease.
Optimizing ion analysis: Ion chromatography with mass
spectrometry
Date: Wednesday, March 18, 2026
Time: 2:00 PM Greenwich Mean Time
Duration: 1 hour
Ion
Chromatography–Mass Spectrometry (IC-MS) offers powerful analytical
capabilities, but optimal sensitivity and long-term performance require
thoughtful system setup. This webinar covers practical strategies for
optimizing IC-MS, focusing on the components and decisions that most strongly
impact routine analysis.
Topics that will be covered include:
- The importance of high-quality eluent
- How the suppressor can affect instrument lifetime
- How to select the right mass spectrometer for your sensitivity needs
- Eluent management strategies to minimize stress on the MS, avoid contamination, and maintain stable performance

Mastering Charged Aerosol Detection (CAD): Understand, Optimize and Troubleshoot
Date: Thursday, March 19, 2026
This technical webinar
provides an in-depth overview of Charged Aerosol Detection (CAD) and its
application in modern liquid chromatography. The session presents the
fundamental principles and underlying technology of the Charged Aerosol
Detector, delivered by our experts.
Learning Points:
- In-depth technical understanding of CAD technology and critical system parameters
- Practical approaches for optimizing CAD methods based on mobile phase composition and application requirements
- Structured troubleshooting strategies for common CAD performance issues
Why
HPLC-CAD is ideal for quality assurance of APIs and excipients
Date: Wednesday, March 25, 2026
The gold standard of quality assessment of drugs is nowadays an HPLC using a reversed-phase (RP) column chromatography and aqueous buffers, acetonitrile, and/or methanol as mobile phase, combined with a UV detector.
Key learning and takeaways include:
- Explore on the critical yet increasingly complex challenge of impurity profiling of APIs and excipients in pharmaceutical analysis
- Review on enhancement of sensitivity in detection to uncover low-level impurities
- Discover examples for quality assurance by HPLC-CAD analysis




