Webinar Videos
Webinar Videos
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.
Multiple-Attribute Monitoring (MAM) at Peptide or Subunit Levels: Ready for QC
59:41
Multiple Attribute Monitoring (MAM) is a method used to concurrently analyze various critical quality attributes (CQAs) of biotherapeutics.
MAM Deployment for QC Analytical Testing and Substitution of Conventional Analytical Methods
19:37
This presentation comprehensively covers the opportunities and challenges related to the adoption of the MAM method across the entire spectrum, ranging from R&D to commercial QC for the release and stability testing of biotherapeutics.
Oligonucleotide Sequence Confirmation for Quality Control by Micheal Ruhl from BioSpring
21:09
Mass spec is a reliable tool for oligonucleotide quality control. We show techniques on the BioAccord LC-MS System and Vion IMS QTof System to confirm the sequence of RNA and DNA oligo therapeutics covering adjuvant, siRNA, ASO, sgRNA and aptamers.
Functional Beverages – Leveraging Analytical Innovations to Overcome Chromatographic Challenges
59:54
Whether you are developing new beverages or ensuring the quality of your current products, this webinar will provide you with the strategies and technologies to thrive in a dynamic and competitive market.
LC MS Methods for Characterization of Long Oligonucleotides
31:36
Resolution performance of LC and MS techniques is challenged by development of long therapeutic oligonucleotides such sgRNA. We'll discuss the application of a modern method LC for separation and MS characterization of long oligonucleotides.
IVD Enabling Harmonization of Steroid Hormones using MassTrak Steroid Serum Sets - Webinar
39:47
This webinar describes analytically sensitive and robust LC-MS/MS method to measure seven endocrine steroid hormones for routine clinical testing.
WEBINAR | Medical Devices: Regulations and Chemical Characterization
59:48
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.
Hyphenation of non-denaturing chromatographic methods to native mass spectrometry and ion mobility for therapeutic protein characterization
27:36
Presentation given by Anthony Ehkirch, LSMBO, at ASMS 2018
WEBINAR - Elevate Your Workflow By Optimizing Durable Data and Intrinsic Compliance
53:38
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.
Advanced Polymer Chromatography for Polymer Analysis Method Development – Tools and Workflow
55:25
The speaker walks through efficient method development and how it can improve your polymer analysis results. The speaker will also share handy tips on how you can save time and solvent during your analysis, which is something to be excited about!
An Industry Perspective of the Current Regulatory Landscape for Nitrosamines
51:50
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.
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
Multiple-Attribute Monitoring (MAM) at Peptide or Subunit Levels: Ready for QC
Multiple Attribute Monitoring (MAM) is a method used to concurrently analyze various critical quality attributes (CQAs) of biotherapeutics.
59:41
MAM Deployment for QC Analytical Testing and Substitution of Conventional Analytical Methods
This presentation comprehensively covers the opportunities and challenges related to the adoption of the MAM method across the entire spectrum, ranging from R&D to commercial QC for the release and stability testing of biotherapeutics.
19:37
Oligonucleotide Sequence Confirmation for Quality Control by Micheal Ruhl from BioSpring
Mass spec is a reliable tool for oligonucleotide quality control. We show techniques on the BioAccord LC-MS System and Vion IMS QTof System to confirm the sequence of RNA and DNA oligo therapeutics covering adjuvant, siRNA, ASO, sgRNA and aptamers.
21:09
Functional Beverages – Leveraging Analytical Innovations to Overcome Chromatographic Challenges
Whether you are developing new beverages or ensuring the quality of your current products, this webinar will provide you with the strategies and technologies to thrive in a dynamic and competitive market.
59:54
LC MS Methods for Characterization of Long Oligonucleotides
Resolution performance of LC and MS techniques is challenged by development of long therapeutic oligonucleotides such sgRNA. We'll discuss the application of a modern method LC for separation and MS characterization of long oligonucleotides.
31:36
IVD Enabling Harmonization of Steroid Hormones using MassTrak Steroid Serum Sets - Webinar
This webinar describes analytically sensitive and robust LC-MS/MS method to measure seven endocrine steroid hormones for routine clinical testing.
39:47
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
Hyphenation of non-denaturing chromatographic methods to native mass spectrometry and ion mobility for therapeutic protein characterization
Presentation given by Anthony Ehkirch, LSMBO, at ASMS 2018
27:36
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
Advanced Polymer Chromatography for Polymer Analysis Method Development – Tools and Workflow
The speaker walks through efficient method development and how it can improve your polymer analysis results. The speaker will also share handy tips on how you can save time and solvent during your analysis, which is something to be excited about!
55:25
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
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
-
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
-
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
-
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
