About The Event

For pharmaceutical companies, elemental analysis is essential for ensuring product quality, process control, and regulatory compliance, but traditional techniques can often create bottlenecks through lengthy sample preparation, high operating costs, and complex workflows. This webinar explores how X-ray Fluorescence (XRF) is transforming pharmaceutical elemental analysis by providing a faster, safer, and more cost-effective alternative for both API and formulation development. XRF enables sample preparation and measurement in under 30 minutes, requires no acid digestion, and can be performed by laboratory technicians with minimal training, helping organizations accelerate decision-making and shorten time-to-market. Join us to discover how XRF supports elemental impurity screening, catalyst residue monitoring, wear metal detection, and ICH Q3D compliance while reducing dependence on hazardous chemicals, costly consumables, and specialized infrastructure. We will compare XRF with conventional ICP-based methods, discuss real-world pharmaceutical applications, and demonstrate how modern XRF solutions can improve laboratory productivity, sustainability, and operational efficiency. Whether you work in pharmaceutical development, manufacturing, quality control, or regulatory testing, this session will provide practical insights into implementing faster elemental analysis workflows without compromising analytical confidence.