From the heparin contamination crisis to the nitrosamine recalls, pharmaceutical impurities have made headlines for their serious health risks and regulatory consequences. These incidents underscore the importance of understanding how impurities form and ensuring robust systems are in place to identify them early.
Download this article to learn:
- How impurities originate from raw materials, manufacturing reactions, and storage conditions
- Modern analytical techniques that identify and quantify impurities
- Emerging technologies and best practices shaping the future of pharmaceutical quality and safety
