Webinar Videos
Webinar Videos
Similis Bio Enhances Biosimilar Development with Waters Solutions
38:53
Learn how Similis Bio implemented a streamlined mAb subunit LC-MS workflow for Multiple Attribute Monitoring of biosimilar mAb candidates during bioprocessing and development.
Chromatographic Techniques for the Characterization of CQAs in Biosimilars
1:03:24
Critical to the development of a biosimilar is understanding the originator and how its CQAs compare against the biosimilar. Learn about solutions that provide high quality peptide mapping, glycan and charge variant data.
Advancing Technology for Better Medicine with MaxPeak HPS Technology
41:25
Learn how to improve assay robustness and reduce the burden associated with migrating methods downstream in the analysis and monitoring of product quality attributes of biopharmaceuticals.
Robust Multi-Level LC-MS Workflows for Biosimilar Comparability Assessment
48:24
Watch this presentation to learn about the uses of the Xevo G3 QTof mass spectrometer in a case study of biosimilar mAb characterization at intact, subunit, and peptide level.
Automated LC-MS Workflow for CQA Assessment of Protein Therapeutics with Speed and Simplicity for Process Development
1:01:40
Here we demonstrate how sample prep has been greatly simplified and automated to enable rapid LC-MS (intact and subunit) analysis at higher throughput, with less human intervention, all while providing high quality to support process development.
Xevo MRT MS Digital Launch : Pushing the boundaries of science with multi reflecting time-of-flight technology
57:26
Discover the Xevo MRT MS: Performance and Speed Without Compromise. Join Prof. Perdita Barran from the University of Manchester as she discusses her Parkinson’s Disease research and insights from our development team on this incredible technology.
Metabolomics Profiling of Sebum and Serum to Monitor Progression Markers of Parkinson's Disease
22:49
Join world-renowned Professor Perdita Barran from the Institute of Biotechnology as she shares her incredible research into Parkinson's Disease.
PFAS Analysis by EPA 1633 | Building a Comprehensive Capability
44:12
Join Waters Corporation for an insightful webinar on PFAS Analysis by EPA 1633 using LC-MS/MS. Learn essential techniques, best practices, and future advancements in PFAS testing to elevate your lab's capabilities.
LC-MS for RNA Therapeutics to Ensure Product Quality and Process Consistency
41:21
LC-MS for RNA Therapeutics to Ensure Product Quality and Process Consistency
Streamlined mAb Subunit LC-MS Workflow for Multiple Attribute Monitoring of Biosimilar mAb Candidates During Bioprocessing and Development
38:53
Clone selection, early in the development lifecycle, has an outsize impact on the ability to match the quality target product profile (QTPP) for a given product.
Elevating Product Quality - BioAccord in Action Video
25:51
Released N-linked glycan analysis is the gold standard for N-glycan profiling of therapeutic monoclonal antibodies (mAbs) as they play an important role in safety and efficacy.
Expedite Process Development with Automated PQA and Spent Media Analysis with the BioAccord LC-MS System
43:22
Here we show how an automation-assisted at-line LC-MS based Process Analytical Technology (PAT) has been successfully implemented to understand process parameters affecting the mis-paired bispecific antibody ratio.
Similis Bio Enhances Biosimilar Development with Waters Solutions
Learn how Similis Bio implemented a streamlined mAb subunit LC-MS workflow for Multiple Attribute Monitoring of biosimilar mAb candidates during bioprocessing and development.
38:53
Chromatographic Techniques for the Characterization of CQAs in Biosimilars
Critical to the development of a biosimilar is understanding the originator and how its CQAs compare against the biosimilar. Learn about solutions that provide high quality peptide mapping, glycan and charge variant data.
1:03:24
Advancing Technology for Better Medicine with MaxPeak HPS Technology
Learn how to improve assay robustness and reduce the burden associated with migrating methods downstream in the analysis and monitoring of product quality attributes of biopharmaceuticals.
41:25
Robust Multi-Level LC-MS Workflows for Biosimilar Comparability Assessment
Watch this presentation to learn about the uses of the Xevo G3 QTof mass spectrometer in a case study of biosimilar mAb characterization at intact, subunit, and peptide level.
48:24
Automated LC-MS Workflow for CQA Assessment of Protein Therapeutics with Speed and Simplicity for Process Development
Here we demonstrate how sample prep has been greatly simplified and automated to enable rapid LC-MS (intact and subunit) analysis at higher throughput, with less human intervention, all while providing high quality to support process development.
1:01:40
Xevo MRT MS Digital Launch : Pushing the boundaries of science with multi reflecting time-of-flight technology
Discover the Xevo MRT MS: Performance and Speed Without Compromise. Join Prof. Perdita Barran from the University of Manchester as she discusses her Parkinson’s Disease research and insights from our development team on this incredible technology.
57:26
Metabolomics Profiling of Sebum and Serum to Monitor Progression Markers of Parkinson's Disease
Join world-renowned Professor Perdita Barran from the Institute of Biotechnology as she shares her incredible research into Parkinson's Disease.
22:49
PFAS Analysis by EPA 1633 | Building a Comprehensive Capability
Join Waters Corporation for an insightful webinar on PFAS Analysis by EPA 1633 using LC-MS/MS. Learn essential techniques, best practices, and future advancements in PFAS testing to elevate your lab's capabilities.
44:12
LC-MS for RNA Therapeutics to Ensure Product Quality and Process Consistency
LC-MS for RNA Therapeutics to Ensure Product Quality and Process Consistency
41:21
Streamlined mAb Subunit LC-MS Workflow for Multiple Attribute Monitoring of Biosimilar mAb Candidates During Bioprocessing and Development
Clone selection, early in the development lifecycle, has an outsize impact on the ability to match the quality target product profile (QTPP) for a given product.
38:53
Elevating Product Quality - BioAccord in Action Video
Released N-linked glycan analysis is the gold standard for N-glycan profiling of therapeutic monoclonal antibodies (mAbs) as they play an important role in safety and efficacy.
25:51
Expedite Process Development with Automated PQA and Spent Media Analysis with the BioAccord LC-MS System
Here we show how an automation-assisted at-line LC-MS based Process Analytical Technology (PAT) has been successfully implemented to understand process parameters affecting the mis-paired bispecific antibody ratio.
43:22
Recent Webinars
Recent Webinars
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An Industry Perspective of the Current Regulatory Landscape for Nitrosamines
In this webinar, Lance Smallshaw, Head of Compendial Affairs at UCB Pharma S.A. (Belgium), will provide an overview of the regulatory landscape today including recent significant updates related to nitrosamines in human medicines.
51:50
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LC-MS/MS Analysis of Serum Thyroglobulin for Clinical Research
This presentation demonstrates performance of a simplified workflow for offline automated sample prep of Tg using the Andrew+ pipetting robot, followed by LC-MS/MS analysis using the ACQUITY UPLC™ I-Class and Xevo™ TQ Absolute for clinical research.
46:03
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Efficient Sample Preparation: How to Make Sample Prep Steps Easier and Gain in Efficiency
In this session, a number of sample preparation methods will be discussed in terms of their strengths and limitations and suitability for particular forensic toxicology applications.
59:25
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The Future of PFAS Analysis - What Advances are We Making in LC-MS/MS?​
This video discusses the types of methodologies used for both EPA 1633 (Draft) and ASTM 8421-21 (Draft) including best practices to help you navigate sample handling and ways to reduce contamination.
23:02
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Webinar | MSACL Connect Webinar
On-Demand: A New Chapter for Mitochondrial Testing: LC-MS/MS based Ketone Body Panel
38:33
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PFAS and the Challenges in Development of a Direct Injection Method by UPLC-MS/MS
The European Commission has recast its Drinking Water Directive to include monitoring and setting limits on specific PFAS. This webinar discusses a direct injection method to address the additional PFAS mentioned in the directive.
34:02
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PFAS Analysis in Environmental Water Samples
In this video, Jenny Davies, Waters Corporation, explains how you can reach ultimate sensitivity when analyzing PFAS in environmental water samples.
1:02:15
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Looking Into Identification Criteria, Quality Assurance, and Validation Specifics
This presentation describes a practical HRMS approach and proposes suggestions for validation and quality assurance.
42:48
Most Viewed Webinars
Most Viewed Webinars
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WEBINAR | Medical Devices: Regulations and Chemical Characterization
Dr. Andrew Feilden shares key insights into the medical device regulatory landscape and discusses key aspects of extractable and leachable analysis requirements associated with newly revised ISO 10993-18.
59:48
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WEBINAR - Elevate Your Workflow By Optimizing Durable Data and Intrinsic Compliance
In this webinar, Waters data integrity experts demonstrate how Empower Lab Management System (LMS) will help your lab optimize its product workflows to support durable data and intrinsic compliance.
53:38
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An Industry Perspective of the Current Regulatory Landscape for Nitrosamines
In this webinar, Lance Smallshaw, Head of Compendial Affairs at UCB Pharma S.A. (Belgium), will provide an overview of the regulatory landscape today including recent significant updates related to nitrosamines in human medicines.
51:50
-
LC-MS/MS Analysis of Serum Thyroglobulin for Clinical Research
This presentation demonstrates performance of a simplified workflow for offline automated sample prep of Tg using the Andrew+ pipetting robot, followed by LC-MS/MS analysis using the ACQUITY UPLC™ I-Class and Xevo™ TQ Absolute for clinical research.
46:03
-
PFAS and the Challenges in Development of a Direct Injection Method by UPLC-MS/MS
The European Commission has recast its Drinking Water Directive to include monitoring and setting limits on specific PFAS. This webinar discusses a direct injection method to address the additional PFAS mentioned in the directive.
34:02
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WEBINAR - Evaluation of Next Generation Waters QTof MS for Biotherapeutic Characterization
Early evaluation of the Waters Xevo G3 QTof instrument for biopharmaceutical characterization.
32:53
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WEBINAR | Progress on Revision of ICH Q2 and the New Q14 Guidance
Hear from Mary Beth Pelletier from Biogen who discusses the development and lifecycle management of analytical methods. She also discusses the scope and drivers for ICH Q2/Q14, what to expect, and what success will look like.
25:30
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A Live Demonstration of the Empower Software with GPC Option
This workshop shows the advantages of using the Empower GPC option to analyze your polymer samples. Besides compliance and traceability, the complete workflow from sample injection to processing and reporting will be demonstrated live by our experts.
59:01
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Mass Spectrometry Fundamentals (Part 1 of 3): Ion Sources
In part 1 of this 3-part webinar series we focus on the ionization techniques commonly used today and some characteristics of ion source design.
57:22
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Validation of a Method to Screen for Drugs in Blood and Urine Using Liquid Chromatography Quadrupole Time-of-Flight (LC-QTof) Mass Spectrometry
Dr. Alex Lawson of Birmingham Heartlands Hospital discusses how his lab changed the screening protocol for drugs in blood and urine, going from the more traditional technologies such as HPLC, GC-MS, and LC-MS/MS to using high-resolution mass spec.
16:46
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Webinar | A Risk-based Approach to Reviewing Electronic Chromatographic Data and Audit Trails with Data Integrity in Mind
In this webinar, we examine the purpose of audit trails, discuss the records that make up an electronic audit trail, address the requirements to effectively review audit trails, and review challenges and practical approaches of the review process.
1:00:32
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LC System Troubleshooting - Part 3
Additional Examples of a Novel Structured Approach to LC System Troubleshooting with a Focus on Vials
1:02:18
