Agilent Technologies, Inc.

Nervous about regulatory inspections of your laboratory? Fear no more! Attend this two-part webcast to learn what to expect during a regulatory inspection, so that you can prepare with confidence. Our experienced team will simulate an inspection and show you how to handle questions and doubts, and what the inspectors will need to see when reviewing your chromatography data system (CDS) and data integrity training. Part 1: Tuesday, September 15, 2020 China/Singapore/Malaysia/Philippines – 2:00pm Indonesia/Thailand/Vietnam – 1:00pm Australia/New Zealand – 4:00pm Central Europe – 8:00am India – 11:30am Part 2: Thursday, September 17, 2020 China/Singapore/Malaysia/Philippines – 2:00pm Indonesia/Thailand/Vietnam – 1:00pm Australia/New Zealand – 4:00pm Central Europe – 8:00am India – 11:30am On demand available after final airing until Sept. 17, 2021.

This webcast will provide an overview of the key concepts required for successful 2D-LC method development, and several examples of recently developed 2D-LC separations of biomolecules. Live: North America: Thursday, Aug. 27, 2020 at 11am EDT | 8am EDT | 4pm BST | 5pm CEST Asia Pacific: Friday, Aug. 28, 2020 at 8:30am IST | 11am CST | 12pm JST Europe: Friday, Aug. 28, 2020 at 2pm BST | 3pm CEST On demand available after final airing until Sept. 28, 2020

Overcome challenges in analysis of PFAS and mitigation using existing and novel water treatment technologies for the removal of PFAS. Arjun Venkatesan, Associate Director, Center for Clean Water Technology, Stony Brook University discusses the ongoing PFAS research of a certified PFAS testing facility to support statewide monitoring. Live: Europe: Thursday, Mar. 5, 2020 at 2pm GMT | 3pm CET US: Thursday, Mar. 5, 2020 at 1pm EST | 12pm CST | 10am PST Asia Pacific: Friday, Mar. 6, 2020 at 9:30am IST | 12pm CST | 1pm JST On demand available after final airing until Mar. 5, 2021 Register free

A focus on research scientist and analytical chemist, Diana Jaeger, analyzing samples using LC/TQ for River Stone Biotech, a new player in synthetic biology.

• Special considerations when updating software • Data integrity challenges in the cloud environment • Implications of moving to the cloud with respect to audits

• Validating custom calculations • The importance of a second-person review and locking data • How to compile a data-integrity plan · · ·

* Analysis of pesticides in complex food matrices * Nontargeting screening for food adulterants/contaminants * Food authenticity testing with LC/Q-TOF

- A data life cycle for chromatography - What is GDocP? - Understanding data integrity metrics for chromatography

How to address the challenges on biotherapeutic aggregate/fragment analysis using SEC/UV and SEC/MS? Live: North America: Wednesday, Feb. 12, 2020 at 11am EST | 10am CST | 8am PST Asia Pacific: Thursday, Feb. 13, 2020 at 8:30am IST | 11am CST | 12pm JST Europe: Thursday, Feb. 13, 2020 at 2pm GMT | 3pm CET On demand available after final airing until Mar. 12, 2020 Register free

In this webcast we will present Agilent samples to answers workflow solutions for monoclonal antibody characterization. The presentation covers analytical strategies for monitoring CQAs. We will focus on main quality attributes such as charge variants, aggregation, glycosylation, host cell protein impurities and post-translational modifications. Live: Europe: Wednesday, Feb. 5, 2020 at 2pm GMT | 3pm CET US: Wednesday, Feb. 5, 2020 at 2pm EST | 1pm CST | 11am PST On demand available after final airing until Feb. 5, 2021 Register free

• Solutions for comparing innovator and biosimilar mAbs • Biosimilar case studies

• Data security in electronic versus paper environments • Division of responsibilities between users and vendors • Specific payment plans can provide advantages to meet financial goals.

Assessing the glycosylation of biotherapeutics is vital to ensuring the safety and efficacy of the end product. In this ebook, explore a variety of methods for improving this important part of protein characterization.

The ability to predict multiple constituents of a final dosage form in one fast, nondestructive measurement can reduce analysis time and cost significantly.

• Acquiring laboratory equipment raises a number of challenges and concerns. • Specific payment plans can provide advantages to meet financial goals.

Join us for this webcast to learn about when you need to use GC–MS/MS in cannabis pesticide testing, how a single-stream sample preparation amenable to both LC–MS/MS and GC–MS/MS improves robustness and increases productivity, and the latest analytical approaches for the analysis of terpenes and residual solvents in cannabinoid products. Live: Tuesday Jan. 21, 2020 at 2pm EST | 1pm CST | 11am PST Thursday, Jan. 30, 2020 at 2pm EST | 1pm CST | 11am PST On demand available after final airing until Jan. 30, 2021 Register free

This application note demonstrates the development of an SFC separation method for 46 highly polar compounds on different columns using an increased amount of modifier.

This technical overview presents the measurement of the instrument detection limit (IDL) at two different conditions of MRM dwell times.