How Reliable Are Your Impurity Results? Impurity Testing: Build Confidence and Reduce Risk.
19 Nov, 2026 | 10:30 AM CET
Join us for a free, insightful webinar with USP on one of the pharmaceutical industry’s most critical challenges: impurity testing.
Impurities may be introduced during formulation, manufacturing, packaging, or storage. They can compromise product quality, patient safety, regulatory approval and compliance, and time to market. Understanding, identifying, and controlling impurities is therefore more important than ever.
Speakers:
Dr. Christian Zeine, Senior Manager Scientific Affairs, EMEA, United States Pharmacopeia
Dr. Freddi Philippart, Head of BioPharma Sales, Eurofins BioPharma Product Testing Germany
This webinar will cover:
- The evolving landscape of impurities – different types of organic impurities and their sources
- Key guidelines, quality considerations, and the USP framework
- Challenges and limitations of impurity reference materials available in the market
- Nitrosamines, extractables and leachables (E&L), and USP's impurities solutions developed to deliver accuracy, efficiency and compliance
Who should attend?
Professionals working in method development, analytical sciences, quality control, or regulatory support.