Webcasts

The Evolution of Consumables Usage Tracking through SMART Technology

Wednesday, October 27, 2021 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST Laboratory data must be secured and available to support product quality decisions, both at the time of the decision-making and for the full duration of the mandated retention period. It is imperative to have durable data. Durable data includes backup and restore, disaster recovery and business continuity planning, archiving, system administration, and cybersecurity.

Analytical-Scale Prep, Semi-Prep, Process Scale Preparative Chromatography: To Infinity and Beyond!

Tuesday, October 26, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Are you planning to turn your analytical HPLC method into a purification method? Are you converting your analytical-scale purification method to semi-prep or production scale? Learn how to set appropriate purification goals for purity, yield and throughput and what type of equipment will best fit your application.

Monday, October 25, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Register today to expand your knowledge of new and unique GC column solutions for fast GC solutions of persistent organic pollutants like PAH and PCB analysis in food, cannabis, and environmental samples. Learn how new GC column phases can help improve the method run time and sensitivity of your analytical methods, making GC column selection a less painful proposition.

Update Your Pharma Analysis or Be Left in the Dust

***Wednesday, October 20, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST*** In the pharmaceutical industry, speed and accuracy are necessary to stay ahead of the competition, yet many labs still use outdated wet chemistry methods. ***On demand available after final airing until October 20, 2022***

Separation Science: The State Of The Art (On Demand Symposium)

Now available On Demand: What are the latest cutting-edge trends in separation science? Learn about the latest advances in liquid chromatography, hyphenated techniques, column technology, sample preparation, and important application areas from key opinion leaders in the field.

Thursday, October 7, 2021 at 2pm EDT | 1pm CDT| 11am PDT Join us to learn more about applications of direct analysis in real time–mass spectrometry (DART-MS) and its relevance to chemical ecology, forensics chemistry, and imaging mass spectrometry.

Wednesday, October 6, 2021 at 12pm EDT | 9am PDT | 5pm BST | 6pm CEST In this webinar, you will learn about the possibility of GMP method transfer for HCP assays leveraging a robust and automated workflow based on combining data-dependent and data-independent mass spectrometry. A study of data from multiple projects over three years demonstrated the robustness and reproducibility of the method.

The Power of CE–MS in Biotherapeutics Characterization

Friday, October 1, 2021 at 10am EDT | 3pm BST | 4pm CEST Characterization of biologics, especially mAbs, can be challenging and time consuming.. Learn how CE–MS offers a superior solution for separation of charge variants and how Transcenta implemented ZipChip CE–MS to achieve a workflow 100x faster than LC–MS.

Airing 1 & 2: Wednesday, September 29, 2021 at 8am EDT | 12pm BST | 1pm CEST and at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Please join Matthew Przybyciel and Kathryn Lawson-Wood as we breakdown the fundamentals in HPLC troubleshooting to increase your lab efficiencies and provide the tools for repeatable, reliable results – time after time. Register and tune in with us on September 29th, 2021.

In the last few years, the issuance of the ISO 10993-18:2020 medical device guidance and several high-profile publications and round-robin studies have resulted in the FDA increasing scrutiny of E&L analyses for both drugs and devices. Join our panel of industry experts to discuss these changes and to learn the direction E&L may take into the future.

Tuesday, September 28, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST In the last few years, the issuance of the ISO 10993-18:2020 medical device guidance and several high-profile publications and round-robin studies have resulted in the FDA increasing scrutiny of E&L analyses for both drugs and devices. Join our panel of industry experts to discuss these changes and to learn the direction E&L may take into the future.

The Evolution of Consumables Usage Tracking through SMART Technology

Monday, September 27, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Reducing instrument downtime is a prime objective for analytical laboratories looking to improve productivity. This webcast will highlight new SMART technology modern laboratories are employing for consumable usage tracking, performing scheduled maintenance and optimizing instrument use for variable sample loads and conditions, while ensuring safe and error-free operations.

Wednesday, September 15, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Size exclusion chromatography (SEC) is a well-established analytical method for quantitative and qualitative aggregate analysis of monoclonal antibodies (mAbs) and other related biotherapeutics.

Tuesday, September 7, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Join us for this webcast to learn an approach to enhance the determination of PFAS in environmental water matrices. This webinar presents a procedure for the detection of adsorbed organically bound fluorine (AOF) by means of combustion ion chromatography (CIC) developed with the aim to establish a rapid and fully automated screening test to complement LC–MS/MS single-substance analysis of PFAS for aqueous environmental matrices.

Tuesday, August 31, 2021 at 11am CEST | 10am BST Join us for this webcast to learn how automated, high-throughput MS analysis without any chromatographic separation can provide fast, sensitive, selective, and robust analysis of volatile compounds in polymers, packaging material and natural matrices at trace levels. Topics will cover high-throughput analysis of diverse industrial and natural samples by coupling headspace and thermal desorption to direct SIFT-MS.

Thursday, August 26, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Developing a robust, transferable size-exclusion chromatography (SEC) method for routine testing of mabs and other biotherapeutics can be challenging. Join us for this presentation to learn about SEC method development, with an emphasis on method transfer and sustainability.