Author:
França Leandro de Moura,Pimentel Maria Fernanda,Simões Simone da Silva,Grangeiro Severino,Prats-Montalbán José M.,Ferrer Alberto
Subject
Pharmaceutical Science,General Medicine,Biotechnology
Reference42 articles.
1. Forced degradation and impurity profiling: recent trends in analytical perspectives;Jain;J. Pharm. Biomed. Anal.,2013
2. LC-MS/MS structural characterization of stress degradation products including the development of a stability indicating assay of Darunavir: an anti-HIV drug;Rao;J. Pharm. Biomed. Anal.,2014
3. ICH harmonised tripartite guideline: Q3B (R2) impurities in New Drug Substances, in: International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, 2006.
4. ICH harmonised tripartite guideline: Q1A (R2) Stability Testing of New Drug Substances and Products, in: International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, 2003.
5. Tools and workflow for structure elucidation of drug degradation products;Foti;TrAC, Trends Anal. Chem.,2013
Cited by
14 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献