Residual solvents analysis for the pharmaceutical industry using the Agilent 8697 Headspace Sampler and 8850 GC-FID system

Residual solvents left behind during API manufacturing pose a regulatory challenge for pharmaceutical producers, requiring precise monitoring to ensure product safety and compliance with USP <467> standards.

Discover how a headspace GC system delivers reliable detection, resolution, and quantitation of residual solvents using helium and hydrogen carrier gases, supporting accurate screening and limit testing in pharmaceutical workflows.