Identification and Control of Impurities for Drug Substance Development using LC/MS and GC/MS
Author:
Affiliation:
1. a Chemical Development Department , Boehringer Ingelheim Pharmaceuticals, Inc. , Ridgefield, Connecticut, USA
Publisher
Informa UK Limited
Subject
Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10826070802279426
Reference17 articles.
1. Pharmaceutical Applications of Liquid Chromatography Coupled with Mass Spectrometry (LC/MS)
2. Isolation and Identification of a Major Impurity in a New Bulk Drug Candidate by Preparative LC, ESI-MSn, LC-MS-MS, and NMR
3. Identification of a trace colored impurity in drug substance by preparative liquid chromatography and mass spectrometry
4. Pharmaceutical impurity identification: A case study using a multidisciplinary approach
5. Liquid chromatography–mass spectrometry using the hydrogen/deuterium exchange reaction as a tool for impurity identification in pharmaceutical process development
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