News|Articles|March 19, 2024
Analysis of N-Nitrosodimethylamine (NDMA) Impurity in Rantidine Products
Author(s)Syft Technologies Inc
Quantitative analysis of volatile nitrosamine impurities in drug products is simplified using SIFT-MS and has a 3X throughput advantage over chromatographic methods.
Related Content
Trending on LCGC International
1
How Should You Respond to FDA 483 Observations?
2
Py-GC–MS Reveals Microplastics in Playgrounds
3
Highlights from the HPLC2026 Conference through the Lens of LC Troubleshooting
4
Q-2DMS: Two-Dimensional Mass Spectrometry Extended to Commercial QTOF Platforms
5