This whitepaper provides an overview of the regulatory challenges posed by the detection of nitrosamine impurities in pharmaceutical products.
In this white paper, we provide an overview of the regulatory challenges posed by the detection of nitrosamine impurities in pharmaceutical products. We also highlight the impact of nitrosamine contamination on the industry, industry collaboration, and the publication of research to aid prevention efforts.
Download Now
Asset 7: Changing regulatory environment for nitrosamine impurities
PDF, Size 0 kb
Topics
- AI, analytics and decision support
- Analytical and bioanalysis
- Bioprocessing and biomanufacturing
- Chromatography and separations
- Controlled release and advanced delivery
- Drug Development
- Endotoxin
- Formulation and drug delivery
- GMP and quality management systems (QMS)
- Quality, microbiology and contamination control
- Regulation and compliance
- SGS Life Sciences
- Upstream processing


