Tips and tricks: how to streamline compliance in a regulated pharmaceutical laboratory
Are you bored of validating Excel spreadsheets? Don’t worry, we have you covered! In this webinar, we will learn more about new features and tools to ensure data integrity, and quality control, and save you and your lab time.
We will walk you through how you can maximize SCIEX OS software features to meet regulatory requirements with confidence. In this webinar, you will learn more about new features and tools to ensure data integrity and quality control and save you and your lab time.
What will you learn?
- How to use custom calculations and other SCIEX OS software features to your advantage
- Ensure data integrity with audit trails
- Verify role configuration and access security
- Learn about how our change control support plan can ensure you have the latest version of software fully validated by SCIEX
Who this may interest?
- Managers and Directors running regulated pharmaceutical laboratories
- Scientists performing regulated analysis in the pharmaceutical industry
Jessica Smith, Ph.D.
Senior Market Development Specialist
SCIEX
Jessica joined SCIEX in 2021 as a technical marketing specialist; her responsibilities included managing projects throughout Europe, the Middle East, Africa and India, and creating new technical marketing content. Her current role is Senior Market Development Specialist for software, educating customers on the transition from Analyst software to SCIEX OS software.
Before joining SCIEX, Jessica worked at ThermoFisher Scientific (MA, USA) as an R&D Scientist, where her focus was column development. Jessica also studied for a Ph.D. in materials chemistry for environmental applications.
This webinar was recorded on Tuesday 22 October 2024
In association with:
