Author:
Gavin Peter F.,Olsen Bernard A.
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference22 articles.
1. Pharmaceutical cGMPS for the 21st Century—A risk-based approach, Final report, Department of Health and Human Services, U.S. Food and Drug Administration, September 2004.
2. International Conference on Harmonization Tripartite Guideline “Q8: Pharmaceutical Development” Nov 10, 2005, 1–8.
3. Chromatography in the United States Pharmacopeia, USP 30-NF 25, The USP Convention, Inc., Rockville, MD, 2007 (Chapter 621).
4. Determination of the enantiomer and positional isomer impurities in atomoxetine hydrochloride with liquid chromatography using polysaccharide chiral stationary phases
5. A quality evaluation strategy for multi-sourced active pharmaceutical ingredient (API) starting materials
Cited by
63 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