Regulatory bodies such as ICH, USP, and EP define limits for residual volatile organic chemicals in pharmaceutical formulations. To meet these guidelines, producers must monitor solvent levels in finished products, active ingredients and additives. Agilent's flexible, pre-configured and factory-tested Residual Solvent Analyzers provide quick start-up for accurate and reproducible analysis of Class 1 and Class 2A/B solvent content in pharmaceutical products.
With an inert sample path and excellent thermal zone stability, the Agilent 7697A Headspace Sampler
automates sample handling to provide unsurpassed accuracy and repeatability combined with analytical precision that exceeds USP method requirements. Choose from the 7890-based GC/FID
or GC/FID/MS system configurations designed to meet your specific monitoring requirements.