Elevate Your Quality with Empower™ | Accelerate Your Method Development and Validation with Empower Data Chromatography System

When developing and validating methods the process can be time consuming and filled with manual steps. Empower Chromatography Data System has inherent functionality that you can leverage to speed up method development and validation so you can create quality methods that are durable and transferable.
In this session, we will explore the options available to help you automate and optimize method development and validation.
Key Learning Objectives
- Working with 3D detection to perform peak tracking and determine peak purity
- Detecting and tracking impurities
- Leveraging automated ranking of experimental results using the Scoring Report
- Tracking and trending data during the method development and validation stages
- Automating and streamlining method validation with the Method Validation Manager option for Empower
- Interfacing Method Development Software with Empower
Presenter: Neil Lander (Principal Product Manager, Informatics, Waters Corporation)
Neil has worked for Waters Corporation since 1994 and has held a variety of positions including Technical Support Specialist, Technical Trainer, Manager Customer Education and currently, Principal Marketing Manager focusing on Informatics solutions. He provides internal support for Empower Chromatography Data System and is focused on developing laboratory software solutions that help organizations achieve their scientific and operational objectives. Prior to joining Waters, he was an analytical chemist where he gained experience in both the cosmetics and specialty chemical industries.
Presenter: Tran Pham (Sr. Business Development Manager, Waters Corporation)
Tran is a Sr. Business Development Manager focusing in the small molecule pharma market at Waters Corporation. Her previous work life at Waters consists of two positions – Empower Technical Trainer and Chemistry Consumables Specialist. Her careers outside of Waters were method development, validation, and routine analysis scientist and analytical development manager at generic manufacturing and contract organization companies. She has over 10 years of immediate technical experience and working regulatory knowledge regarding small molecule testing, data quality and data integrity.
