Pharma-Compliant Testing of Elemental Impurities

Testing Pharmaceuticals with ICP-MS, ICP-OES & AAS in Pharma QC

Regulatory requirements for pharmaceutical analytics are becoming stricter. This web seminar shows how elemental analysis using ICP-MS, ICP-OES, and AAS ensures compliance with USP <232>, USP <233>, and other standards. Learn about key method requirements—such as system suitability, accuracy, and specificity—for Class 1, 2, and 3 elements. Practical examples from pharmaceutical quality control illustrate efficient workflows for trace element analysis in drug formulations. AAS will be highlighted for targeted applications like electrolyte solutions. The session also addresses common implementation challenges and demonstrates how to integrate compliant workflows into routine lab operations with minimal complexity.

Duration: ~40 min
Language: English
Speakers:
Franz Lehmann, Application Specialist ICP MS
Holger Sievers, Product Manager AAS

Key Topics:
- Overview of USP <232> and <233>
- Practical insights into ICP-OES, ICP-MS and AAS
- Technology comparison: strengths, limitations, and application areas
- Live Q&A with our application experts

Learn more: Visit our website for full details on the web seminar.