Analytical Strategies for USP Residual Solvents Analysis

In this presentation, we will present the relevant GC/FID and GC/FID/MS based analytical strategies to confidently detect and quantify Class 1, 2, and 3 as well as unknown solvents in drug products. Learn how taking advantage of dual channel configuration and Agilent’s Smart, Connected, and Self-Aware systems can help you successfully meet your requirements for residual solvent analysis and ensure your testing is right first time and every time.

 

What will you learn

• Understand what residual solvent impurities are and why it’s important to characterise and quantify them, even when present in trace amounts
• Understand the current regulatory guidelines for residual solvent analysis in drug substance and product
• Learn about the approaches for the confident identification and quantification of residual solvents

 

Who should attend this webinar

• Laboratory managers
• Chromatographers
• Analytical chemists and scientists
• New product developers
• Pharma quality control managers

 

Speaker