Join us for a focused session on the detection of toxic impurities – diethylene glycol (DEG) and ethylene glycol (EG) – in oral liquid pharmaceuticals using High-Performance Thin-Layer Chromatography (HPTLC). You’ll learn about the regulatory background, optimized sample preparation and chromatographic methods, and how CAMAG’s HPTLC system enables rapid, cost-effective, and visual detection at trace levels.
Key Learning Objectives:
- Understand the public health risks and regulatory requirements related to DEG and EG contamination in pharmaceutical syrups.
- Learn how to perform sample preparation, chromatographic separation, and derivatization for DEG/EG detection using HPTLC.
- Gain insights into method parameters, including limit of detection (LOD) and quantification (LOQ).
- Discover how CAMAG’s HPTLC platform facilitates high-throughput, cost-effective, and visual impurity profiling for routine quality control application
Who should attend?
- Quality Control Analysts
- Pharmaceutical Manufacturers
- Regulatory Officers
- Lab technicians
Speakers
Dr. Tiên Do
Chief Scientific Officer
CAMAG
Sonja Drobnjak
Scientist
CAMAG