LCMS webinars focusing on Academy/Principles - page 2

How To Start Up and Shut Down LC and LC-MS Instruments

How To Start Up and Shut Down LC and LC-MS Instruments

Learn practical LC and LC-MS startup and shutdown procedures, column care, and system checks in this webinar. Gain system-agnostic best practices to protect instruments and maximize column lifetime.
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Already taken place We, 6.5.2026
Phenomenex
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How To Start Up and Shut Down LC and LC-MS Instruments
The Basics of Titration explained

The Basics of Titration explained

In this webinar, Robert Tobler, Senior Application Specialist Titration at Metrohm International Headquarters, will give you an introduction to the basics of titration.
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Already taken place We, 29.4.2026
Metrohm
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The Basics of Titration explained
Fundamentals First Bio Series – SEC for Biologics

Fundamentals First Bio Series – SEC for Biologics

Master SEC fundamentals for biopharma—covering principles, column selection, and troubleshooting with real-world applications in mAbs, AAVs, and nucleic acids.
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Already taken place We, 29.4.2026
Phenomenex
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Fundamentals First Bio Series – SEC for Biologics
Tosoh Tuesday - What is MALS & When is it Useful?

Tosoh Tuesday - What is MALS & When is it Useful?

Join Tosoh Tuesday to explore MALS fundamentals, practical implementation, and real-world SEC-MALS applications for polymer and biologics characterization.
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Already taken place Tu, 28.4.2026
Tosoh Bioscience
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Tosoh Tuesday - What is MALS & When is it Useful?
Managing Process Performance in Stage 3 Process Validation: Regulatory Expectations for Continued Process Verification

Managing Process Performance in Stage 3 Process Validation: Regulatory Expectations for Continued Process Verification

Join this webinar to gain practical insights into regulatory expectations for CPV and strengthen your approach to maintaining process performance throughout the product lifecycle.
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Already taken place Th, 23.4.2026
Waters Corporation
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Managing Process Performance in Stage 3 Process Validation: Regulatory Expectations for Continued Process Verification
Biopharma fundamentals: LCMS Biopharma characterization

Biopharma fundamentals: LCMS Biopharma characterization

Join the Biopharma Fundamentals masterclass to learn practical LC-MS strategies for protein identity, purity, sequence, and PTM characterization in biopharmaceutical workflows.
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Already taken place Fr, 6.3.2026
SCIEX
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Biopharma fundamentals: LCMS Biopharma characterization
Understanding and Applying USP Chapter 621 for Generic Pharmaceutical Applications

Understanding and Applying USP Chapter 621 for Generic Pharmaceutical Applications

This webinar will cover the guidelines defined in <621> and provide practical examples of how to apply them.
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Already taken place We, 18.2.2026
Phenomenex
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Understanding and Applying USP Chapter 621 for Generic Pharmaceutical Applications
LC Method Transfer: Hidden Challenges & Absolute Solution

LC Method Transfer: Hidden Challenges & Absolute Solution

Discover why LC method transfer between legacy and modern systems is challenging. Learn which hidden parameters affect retention, peak shape, and robustness—and how to achieve reliable results.
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Already taken place Fr, 13.2.2026
Agilent Technologies
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LC Method Transfer: Hidden Challenges & Absolute Solution
Screening Demystified: Practical Guidelines for Getting It Right with High-Resolution Part 2: How to Set-Up for Success

Screening Demystified: Practical Guidelines for Getting It Right with High-Resolution Part 2: How to Set-Up for Success

Learn how to set up HRMS screening for success. Explore instrument capabilities, software tools, validation strategies, and workflow design to achieve reliable, unbiased LC/QTOF screening results.
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Already taken place Th, 5.2.2026
Agilent Technologies
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Screening Demystified: Practical Guidelines for Getting It Right with High-Resolution Part 2: How to Set-Up for Success
Screening Demystified: Practical Guidelines for Getting It Right with High-Resolution Part 1: All About Screening

Screening Demystified: Practical Guidelines for Getting It Right with High-Resolution Part 1: All About Screening

Demystify high-resolution LC/MS screening. Learn how to design reliable HRMS workflows, avoid false results, and unlock the full potential of LC/QTOF screening for complex analytical applications.
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Already taken place Tu, 3.2.2026
Agilent Technologies
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Screening Demystified: Practical Guidelines for Getting It Right with High-Resolution Part 1: All About Screening
 

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