Improving Method Transfer Outcomes with Intuitive Innovation
Solving Problems that Matter: Risk Mitigation in the Pharma QC Laboratory
Expert Insights 3-Part Webinar Series: Risk Assessment, Control Strategies, and Intuitive Innovation to Improve Data Quality, Data Integrity and Lab Productivity.
Pharma QC labs are facing increasing pressure on the cost of quality while maintaining compliance and assuring patient safety. From the harmonization of USP <621> to Empower™ workflows supporting data integrity to improving method transfer outcomes, you will learn from subject matter experts how to reduce errors and mitigate risk for reproducible data and enhanced productivity.
Who should attend
- Pharma QC Lab directors, managers and senior scientists with a drive to reduce errors, improve lab productivity and enhance data quality & integrity.
PART 2 l Improving Method Transfer Outcomes with Intuitive Innovation
- Wednesday, August 16th, 11:30-12:30 ET
Your LC systems need to support both legacy and new methods that can be operated repeatably anywhere in the world while meeting regulatory requirements. These requirements can also place a large burden on your analysts, but failing to perform necessary tasks could put your organization at risk.
This webinar will introduce our latest HPLC innovation – the Alliance iS HPLC System – that features improved enhanced temperature control to match global needs. Additional features include our intelligent method translator app (iMTA), method matching app, system audit trail and automated column history tracking.
Presenter: Lise Gauthier (Principal Scientist, Waters Corproation)
Lise Gauthier is Principal Scientist within the QA/QC Business Strategy group at Waters Corporation in Milford, MA. Prior to joining Waters in 2014, Lise worked as a scientist as Astra Zeneca for 20 years holding positions of increasing responsibility within Quality Assurance and Drug Discovery. Her current role at Waters includes system validation and evaluation of competitive systems.
