Are you navigating ICH M10 requirements for your regulated bioanalysis workflows?
Join our experts as we break down the globally harmonized ICH M10 guidelines, show how labs are applying them in practice, and explore how SCIEX OS software helps ensure quality, efficiency, and compliance.
What you’ll learn:
- What the ICH M10 guideline is and why it matters for regulated bioanalysis
- How pharmaceutical labs are approaching method validation and study sample analysis
- Common workflow challenges and inefficiencies in meeting regulatory expectations
- How SCIEX OS software simplifies data management, calculations, and reporting
- A live demonstration of current calculation workflows using SCIEX OS software
- A vision for the future of streamlined bioanalytical validation
Henri Meijering, Ardena
Henri Meijering is a seasoned bioanalytical scientist with over 20 years of experience in drug development and pharmacokinetics. He specializes in developing and validating LC-MS/MS and HPLC methods for both small and large molecules. At Ardena Bioanalytical Laboratory, Henri leads scientific strategy and supports complex studies as Business Support Manager. A former core member of the EBF during the ICH M10 rollout, he is passionate about advancing scientific rigor and compliance in regulated bioanalysis.
Heather Hughes, SCIEX
Heather Hughes holds a degree in chemistry from Durham University and has built a career spanning clinical and pharmaceutical science. They began in NHS hospital laboratories, specializing in clinical chemistry, before moving into the pharmaceutical industry with experience at Pfizer and a contract research organization. With a background in both regulated and non-regulated environments, they joined SCIEX nine years ago as an application specialist. In this role, they support customers through training, troubleshooting, and showcasing SCIEX mass spectrometry solutions for small molecule workflows.